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1.

rs1491497062 has merged into rs11312564 [Homo sapiens]
    Variant type:
    DELINS
    Alleles:
    TTTTTTTTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
    Chromosome:
    10:95869251 (GRCh38)
    10:97629008 (GRCh37)
    Canonical SPDI:
    NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:95869241:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
    Gene:
    ENTPD1 (Varview), ENTPD1-AS1 (Varview)
    Functional Consequence:
    intron_variant,genic_downstream_transcript_variant,3_prime_UTR_variant
    Validated:
    by frequency,by alfa,by cluster
    MAF:
    TTTTTTTTT=0./0 (ALFA)
    HGVS:
    NC_000010.11:g.95869251_95869267del, NC_000010.11:g.95869253_95869267del, NC_000010.11:g.95869254_95869267del, NC_000010.11:g.95869255_95869267del, NC_000010.11:g.95869256_95869267del, NC_000010.11:g.95869257_95869267del, NC_000010.11:g.95869258_95869267del, NC_000010.11:g.95869259_95869267del, NC_000010.11:g.95869260_95869267del, NC_000010.11:g.95869261_95869267del, NC_000010.11:g.95869262_95869267del, NC_000010.11:g.95869263_95869267del, NC_000010.11:g.95869264_95869267del, NC_000010.11:g.95869265_95869267del, NC_000010.11:g.95869266_95869267del, NC_000010.11:g.95869267del, NC_000010.11:g.95869267dup, NC_000010.11:g.95869266_95869267dup, NC_000010.11:g.95869265_95869267dup, NC_000010.11:g.95869264_95869267dup, NC_000010.11:g.95869263_95869267dup, NC_000010.11:g.95869262_95869267dup, NC_000010.11:g.95869261_95869267dup, NC_000010.11:g.95869260_95869267dup, NC_000010.11:g.95869258_95869267dup, NC_000010.11:g.95869256_95869267dup, NC_000010.11:g.95869255_95869267dup, NC_000010.11:g.95869253_95869267dup, NC_000010.11:g.95869252_95869267dup, NC_000010.11:g.95869251_95869267dup, NC_000010.11:g.95869248_95869267dup, NC_000010.11:g.95869247_95869267dup, NC_000010.11:g.95869246_95869267dup, NC_000010.11:g.95869245_95869267dup, NC_000010.11:g.95869244_95869267dup, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.95869267_95869268insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629008_97629024del, NC_000010.10:g.97629010_97629024del, NC_000010.10:g.97629011_97629024del, NC_000010.10:g.97629012_97629024del, NC_000010.10:g.97629013_97629024del, NC_000010.10:g.97629014_97629024del, NC_000010.10:g.97629015_97629024del, NC_000010.10:g.97629016_97629024del, NC_000010.10:g.97629017_97629024del, NC_000010.10:g.97629018_97629024del, NC_000010.10:g.97629019_97629024del, NC_000010.10:g.97629020_97629024del, NC_000010.10:g.97629021_97629024del, NC_000010.10:g.97629022_97629024del, NC_000010.10:g.97629023_97629024del, NC_000010.10:g.97629024del, NC_000010.10:g.97629024dup, NC_000010.10:g.97629023_97629024dup, NC_000010.10:g.97629022_97629024dup, NC_000010.10:g.97629021_97629024dup, NC_000010.10:g.97629020_97629024dup, NC_000010.10:g.97629019_97629024dup, NC_000010.10:g.97629018_97629024dup, NC_000010.10:g.97629017_97629024dup, NC_000010.10:g.97629015_97629024dup, NC_000010.10:g.97629013_97629024dup, NC_000010.10:g.97629012_97629024dup, NC_000010.10:g.97629010_97629024dup, NC_000010.10:g.97629009_97629024dup, NC_000010.10:g.97629008_97629024dup, NC_000010.10:g.97629005_97629024dup, NC_000010.10:g.97629004_97629024dup, NC_000010.10:g.97629003_97629024dup, NC_000010.10:g.97629002_97629024dup, NC_000010.10:g.97629001_97629024dup, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.97629024_97629025insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162473_162489del, NG_042803.1:g.162475_162489del, NG_042803.1:g.162476_162489del, NG_042803.1:g.162477_162489del, NG_042803.1:g.162478_162489del, NG_042803.1:g.162479_162489del, NG_042803.1:g.162480_162489del, NG_042803.1:g.162481_162489del, NG_042803.1:g.162482_162489del, NG_042803.1:g.162483_162489del, NG_042803.1:g.162484_162489del, NG_042803.1:g.162485_162489del, NG_042803.1:g.162486_162489del, NG_042803.1:g.162487_162489del, NG_042803.1:g.162488_162489del, NG_042803.1:g.162489del, NG_042803.1:g.162489dup, NG_042803.1:g.162488_162489dup, NG_042803.1:g.162487_162489dup, NG_042803.1:g.162486_162489dup, NG_042803.1:g.162485_162489dup, NG_042803.1:g.162484_162489dup, NG_042803.1:g.162483_162489dup, NG_042803.1:g.162482_162489dup, NG_042803.1:g.162480_162489dup, NG_042803.1:g.162478_162489dup, NG_042803.1:g.162477_162489dup, NG_042803.1:g.162475_162489dup, NG_042803.1:g.162474_162489dup, NG_042803.1:g.162473_162489dup, NG_042803.1:g.162470_162489dup, NG_042803.1:g.162469_162489dup, NG_042803.1:g.162468_162489dup, NG_042803.1:g.162467_162489dup, NG_042803.1:g.162466_162489dup, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_042803.1:g.162489_162490insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2868_*2884del, NM_001776.6:c.*2870_*2884del, NM_001776.6:c.*2871_*2884del, NM_001776.6:c.*2872_*2884del, NM_001776.6:c.*2873_*2884del, NM_001776.6:c.*2874_*2884del, NM_001776.6:c.*2875_*2884del, NM_001776.6:c.*2876_*2884del, NM_001776.6:c.*2877_*2884del, NM_001776.6:c.*2878_*2884del, NM_001776.6:c.*2879_*2884del, NM_001776.6:c.*2880_*2884del, NM_001776.6:c.*2881_*2884del, NM_001776.6:c.*2882_*2884del, NM_001776.6:c.*2883_*2884del, NM_001776.6:c.*2884del, NM_001776.6:c.*2884dup, NM_001776.6:c.*2883_*2884dup, NM_001776.6:c.*2882_*2884dup, NM_001776.6:c.*2881_*2884dup, NM_001776.6:c.*2880_*2884dup, NM_001776.6:c.*2879_*2884dup, NM_001776.6:c.*2878_*2884dup, NM_001776.6:c.*2877_*2884dup, NM_001776.6:c.*2875_*2884dup, NM_001776.6:c.*2873_*2884dup, NM_001776.6:c.*2872_*2884dup, NM_001776.6:c.*2870_*2884dup, NM_001776.6:c.*2869_*2884dup, NM_001776.6:c.*2868_*2884dup, NM_001776.6:c.*2865_*2884dup, NM_001776.6:c.*2864_*2884dup, NM_001776.6:c.*2863_*2884dup, NM_001776.6:c.*2862_*2884dup, NM_001776.6:c.*2861_*2884dup, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.6:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2868_*2884del, NM_001776.5:c.*2870_*2884del, NM_001776.5:c.*2871_*2884del, NM_001776.5:c.*2872_*2884del, NM_001776.5:c.*2873_*2884del, NM_001776.5:c.*2874_*2884del, NM_001776.5:c.*2875_*2884del, NM_001776.5:c.*2876_*2884del, NM_001776.5:c.*2877_*2884del, NM_001776.5:c.*2878_*2884del, NM_001776.5:c.*2879_*2884del, NM_001776.5:c.*2880_*2884del, NM_001776.5:c.*2881_*2884del, NM_001776.5:c.*2882_*2884del, NM_001776.5:c.*2883_*2884del, NM_001776.5:c.*2884del, NM_001776.5:c.*2884dup, NM_001776.5:c.*2883_*2884dup, NM_001776.5:c.*2882_*2884dup, NM_001776.5:c.*2881_*2884dup, NM_001776.5:c.*2880_*2884dup, NM_001776.5:c.*2879_*2884dup, NM_001776.5:c.*2878_*2884dup, NM_001776.5:c.*2877_*2884dup, NM_001776.5:c.*2875_*2884dup, NM_001776.5:c.*2873_*2884dup, NM_001776.5:c.*2872_*2884dup, NM_001776.5:c.*2870_*2884dup, NM_001776.5:c.*2869_*2884dup, NM_001776.5:c.*2868_*2884dup, NM_001776.5:c.*2865_*2884dup, NM_001776.5:c.*2864_*2884dup, NM_001776.5:c.*2863_*2884dup, NM_001776.5:c.*2862_*2884dup, NM_001776.5:c.*2861_*2884dup, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001776.5:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2868_*2884del, NM_001098175.2:c.*2870_*2884del, NM_001098175.2:c.*2871_*2884del, NM_001098175.2:c.*2872_*2884del, NM_001098175.2:c.*2873_*2884del, NM_001098175.2:c.*2874_*2884del, NM_001098175.2:c.*2875_*2884del, NM_001098175.2:c.*2876_*2884del, NM_001098175.2:c.*2877_*2884del, NM_001098175.2:c.*2878_*2884del, NM_001098175.2:c.*2879_*2884del, NM_001098175.2:c.*2880_*2884del, NM_001098175.2:c.*2881_*2884del, NM_001098175.2:c.*2882_*2884del, NM_001098175.2:c.*2883_*2884del, NM_001098175.2:c.*2884del, NM_001098175.2:c.*2884dup, NM_001098175.2:c.*2883_*2884dup, NM_001098175.2:c.*2882_*2884dup, NM_001098175.2:c.*2881_*2884dup, NM_001098175.2:c.*2880_*2884dup, NM_001098175.2:c.*2879_*2884dup, NM_001098175.2:c.*2878_*2884dup, NM_001098175.2:c.*2877_*2884dup, NM_001098175.2:c.*2875_*2884dup, NM_001098175.2:c.*2873_*2884dup, NM_001098175.2:c.*2872_*2884dup, NM_001098175.2:c.*2870_*2884dup, NM_001098175.2:c.*2869_*2884dup, NM_001098175.2:c.*2868_*2884dup, NM_001098175.2:c.*2865_*2884dup, NM_001098175.2:c.*2864_*2884dup, NM_001098175.2:c.*2863_*2884dup, NM_001098175.2:c.*2862_*2884dup, NM_001098175.2:c.*2861_*2884dup, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2868_*2884del, NM_001098175.1:c.*2870_*2884del, NM_001098175.1:c.*2871_*2884del, NM_001098175.1:c.*2872_*2884del, NM_001098175.1:c.*2873_*2884del, NM_001098175.1:c.*2874_*2884del, NM_001098175.1:c.*2875_*2884del, NM_001098175.1:c.*2876_*2884del, NM_001098175.1:c.*2877_*2884del, NM_001098175.1:c.*2878_*2884del, NM_001098175.1:c.*2879_*2884del, NM_001098175.1:c.*2880_*2884del, NM_001098175.1:c.*2881_*2884del, NM_001098175.1:c.*2882_*2884del, NM_001098175.1:c.*2883_*2884del, NM_001098175.1:c.*2884del, NM_001098175.1:c.*2884dup, NM_001098175.1:c.*2883_*2884dup, NM_001098175.1:c.*2882_*2884dup, NM_001098175.1:c.*2881_*2884dup, NM_001098175.1:c.*2880_*2884dup, NM_001098175.1:c.*2879_*2884dup, NM_001098175.1:c.*2878_*2884dup, NM_001098175.1:c.*2877_*2884dup, NM_001098175.1:c.*2875_*2884dup, NM_001098175.1:c.*2873_*2884dup, NM_001098175.1:c.*2872_*2884dup, NM_001098175.1:c.*2870_*2884dup, NM_001098175.1:c.*2869_*2884dup, NM_001098175.1:c.*2868_*2884dup, NM_001098175.1:c.*2865_*2884dup, NM_001098175.1:c.*2864_*2884dup, NM_001098175.1:c.*2863_*2884dup, NM_001098175.1:c.*2862_*2884dup, NM_001098175.1:c.*2861_*2884dup, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001098175.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2868_*2884del, NM_001164179.2:c.*2870_*2884del, NM_001164179.2:c.*2871_*2884del, NM_001164179.2:c.*2872_*2884del, NM_001164179.2:c.*2873_*2884del, NM_001164179.2:c.*2874_*2884del, NM_001164179.2:c.*2875_*2884del, NM_001164179.2:c.*2876_*2884del, NM_001164179.2:c.*2877_*2884del, NM_001164179.2:c.*2878_*2884del, NM_001164179.2:c.*2879_*2884del, NM_001164179.2:c.*2880_*2884del, NM_001164179.2:c.*2881_*2884del, NM_001164179.2:c.*2882_*2884del, NM_001164179.2:c.*2883_*2884del, NM_001164179.2:c.*2884del, NM_001164179.2:c.*2884dup, NM_001164179.2:c.*2883_*2884dup, NM_001164179.2:c.*2882_*2884dup, NM_001164179.2:c.*2881_*2884dup, NM_001164179.2:c.*2880_*2884dup, NM_001164179.2:c.*2879_*2884dup, NM_001164179.2:c.*2878_*2884dup, NM_001164179.2:c.*2877_*2884dup, NM_001164179.2:c.*2875_*2884dup, NM_001164179.2:c.*2873_*2884dup, NM_001164179.2:c.*2872_*2884dup, NM_001164179.2:c.*2870_*2884dup, NM_001164179.2:c.*2869_*2884dup, NM_001164179.2:c.*2868_*2884dup, NM_001164179.2:c.*2865_*2884dup, NM_001164179.2:c.*2864_*2884dup, NM_001164179.2:c.*2863_*2884dup, NM_001164179.2:c.*2862_*2884dup, NM_001164179.2:c.*2861_*2884dup, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2868_*2884del, NM_001164179.1:c.*2870_*2884del, NM_001164179.1:c.*2871_*2884del, NM_001164179.1:c.*2872_*2884del, NM_001164179.1:c.*2873_*2884del, NM_001164179.1:c.*2874_*2884del, NM_001164179.1:c.*2875_*2884del, NM_001164179.1:c.*2876_*2884del, NM_001164179.1:c.*2877_*2884del, NM_001164179.1:c.*2878_*2884del, NM_001164179.1:c.*2879_*2884del, NM_001164179.1:c.*2880_*2884del, NM_001164179.1:c.*2881_*2884del, NM_001164179.1:c.*2882_*2884del, NM_001164179.1:c.*2883_*2884del, NM_001164179.1:c.*2884del, NM_001164179.1:c.*2884dup, NM_001164179.1:c.*2883_*2884dup, NM_001164179.1:c.*2882_*2884dup, NM_001164179.1:c.*2881_*2884dup, NM_001164179.1:c.*2880_*2884dup, NM_001164179.1:c.*2879_*2884dup, NM_001164179.1:c.*2878_*2884dup, NM_001164179.1:c.*2877_*2884dup, NM_001164179.1:c.*2875_*2884dup, NM_001164179.1:c.*2873_*2884dup, NM_001164179.1:c.*2872_*2884dup, NM_001164179.1:c.*2870_*2884dup, NM_001164179.1:c.*2869_*2884dup, NM_001164179.1:c.*2868_*2884dup, NM_001164179.1:c.*2865_*2884dup, NM_001164179.1:c.*2864_*2884dup, NM_001164179.1:c.*2863_*2884dup, NM_001164179.1:c.*2862_*2884dup, NM_001164179.1:c.*2861_*2884dup, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164179.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2868_*2884del, NM_001164182.2:c.*2870_*2884del, NM_001164182.2:c.*2871_*2884del, NM_001164182.2:c.*2872_*2884del, NM_001164182.2:c.*2873_*2884del, NM_001164182.2:c.*2874_*2884del, NM_001164182.2:c.*2875_*2884del, NM_001164182.2:c.*2876_*2884del, NM_001164182.2:c.*2877_*2884del, NM_001164182.2:c.*2878_*2884del, NM_001164182.2:c.*2879_*2884del, NM_001164182.2:c.*2880_*2884del, NM_001164182.2:c.*2881_*2884del, NM_001164182.2:c.*2882_*2884del, NM_001164182.2:c.*2883_*2884del, NM_001164182.2:c.*2884del, NM_001164182.2:c.*2884dup, NM_001164182.2:c.*2883_*2884dup, NM_001164182.2:c.*2882_*2884dup, NM_001164182.2:c.*2881_*2884dup, NM_001164182.2:c.*2880_*2884dup, NM_001164182.2:c.*2879_*2884dup, NM_001164182.2:c.*2878_*2884dup, NM_001164182.2:c.*2877_*2884dup, NM_001164182.2:c.*2875_*2884dup, NM_001164182.2:c.*2873_*2884dup, NM_001164182.2:c.*2872_*2884dup, NM_001164182.2:c.*2870_*2884dup, NM_001164182.2:c.*2869_*2884dup, NM_001164182.2:c.*2868_*2884dup, NM_001164182.2:c.*2865_*2884dup, NM_001164182.2:c.*2864_*2884dup, NM_001164182.2:c.*2863_*2884dup, NM_001164182.2:c.*2862_*2884dup, NM_001164182.2:c.*2861_*2884dup, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2868_*2884del, NM_001164182.1:c.*2870_*2884del, NM_001164182.1:c.*2871_*2884del, NM_001164182.1:c.*2872_*2884del, NM_001164182.1:c.*2873_*2884del, NM_001164182.1:c.*2874_*2884del, NM_001164182.1:c.*2875_*2884del, NM_001164182.1:c.*2876_*2884del, NM_001164182.1:c.*2877_*2884del, NM_001164182.1:c.*2878_*2884del, NM_001164182.1:c.*2879_*2884del, NM_001164182.1:c.*2880_*2884del, NM_001164182.1:c.*2881_*2884del, NM_001164182.1:c.*2882_*2884del, NM_001164182.1:c.*2883_*2884del, NM_001164182.1:c.*2884del, NM_001164182.1:c.*2884dup, NM_001164182.1:c.*2883_*2884dup, NM_001164182.1:c.*2882_*2884dup, NM_001164182.1:c.*2881_*2884dup, NM_001164182.1:c.*2880_*2884dup, NM_001164182.1:c.*2879_*2884dup, NM_001164182.1:c.*2878_*2884dup, NM_001164182.1:c.*2877_*2884dup, NM_001164182.1:c.*2875_*2884dup, NM_001164182.1:c.*2873_*2884dup, NM_001164182.1:c.*2872_*2884dup, NM_001164182.1:c.*2870_*2884dup, NM_001164182.1:c.*2869_*2884dup, NM_001164182.1:c.*2868_*2884dup, NM_001164182.1:c.*2865_*2884dup, NM_001164182.1:c.*2864_*2884dup, NM_001164182.1:c.*2863_*2884dup, NM_001164182.1:c.*2862_*2884dup, NM_001164182.1:c.*2861_*2884dup, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164182.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2868_*2884del, NM_001164183.2:c.*2870_*2884del, NM_001164183.2:c.*2871_*2884del, NM_001164183.2:c.*2872_*2884del, NM_001164183.2:c.*2873_*2884del, NM_001164183.2:c.*2874_*2884del, NM_001164183.2:c.*2875_*2884del, NM_001164183.2:c.*2876_*2884del, NM_001164183.2:c.*2877_*2884del, NM_001164183.2:c.*2878_*2884del, NM_001164183.2:c.*2879_*2884del, NM_001164183.2:c.*2880_*2884del, NM_001164183.2:c.*2881_*2884del, NM_001164183.2:c.*2882_*2884del, NM_001164183.2:c.*2883_*2884del, NM_001164183.2:c.*2884del, NM_001164183.2:c.*2884dup, NM_001164183.2:c.*2883_*2884dup, NM_001164183.2:c.*2882_*2884dup, NM_001164183.2:c.*2881_*2884dup, NM_001164183.2:c.*2880_*2884dup, NM_001164183.2:c.*2879_*2884dup, NM_001164183.2:c.*2878_*2884dup, NM_001164183.2:c.*2877_*2884dup, NM_001164183.2:c.*2875_*2884dup, NM_001164183.2:c.*2873_*2884dup, NM_001164183.2:c.*2872_*2884dup, NM_001164183.2:c.*2870_*2884dup, NM_001164183.2:c.*2869_*2884dup, NM_001164183.2:c.*2868_*2884dup, NM_001164183.2:c.*2865_*2884dup, NM_001164183.2:c.*2864_*2884dup, NM_001164183.2:c.*2863_*2884dup, NM_001164183.2:c.*2862_*2884dup, NM_001164183.2:c.*2861_*2884dup, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2868_*2884del, NM_001164183.1:c.*2870_*2884del, NM_001164183.1:c.*2871_*2884del, NM_001164183.1:c.*2872_*2884del, NM_001164183.1:c.*2873_*2884del, NM_001164183.1:c.*2874_*2884del, NM_001164183.1:c.*2875_*2884del, NM_001164183.1:c.*2876_*2884del, NM_001164183.1:c.*2877_*2884del, NM_001164183.1:c.*2878_*2884del, NM_001164183.1:c.*2879_*2884del, NM_001164183.1:c.*2880_*2884del, NM_001164183.1:c.*2881_*2884del, NM_001164183.1:c.*2882_*2884del, NM_001164183.1:c.*2883_*2884del, NM_001164183.1:c.*2884del, NM_001164183.1:c.*2884dup, NM_001164183.1:c.*2883_*2884dup, NM_001164183.1:c.*2882_*2884dup, NM_001164183.1:c.*2881_*2884dup, NM_001164183.1:c.*2880_*2884dup, NM_001164183.1:c.*2879_*2884dup, NM_001164183.1:c.*2878_*2884dup, NM_001164183.1:c.*2877_*2884dup, NM_001164183.1:c.*2875_*2884dup, NM_001164183.1:c.*2873_*2884dup, NM_001164183.1:c.*2872_*2884dup, NM_001164183.1:c.*2870_*2884dup, NM_001164183.1:c.*2869_*2884dup, NM_001164183.1:c.*2868_*2884dup, NM_001164183.1:c.*2865_*2884dup, NM_001164183.1:c.*2864_*2884dup, NM_001164183.1:c.*2863_*2884dup, NM_001164183.1:c.*2862_*2884dup, NM_001164183.1:c.*2861_*2884dup, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164183.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2868_*2884del, NM_001312654.1:c.*2870_*2884del, NM_001312654.1:c.*2871_*2884del, NM_001312654.1:c.*2872_*2884del, NM_001312654.1:c.*2873_*2884del, NM_001312654.1:c.*2874_*2884del, NM_001312654.1:c.*2875_*2884del, NM_001312654.1:c.*2876_*2884del, NM_001312654.1:c.*2877_*2884del, NM_001312654.1:c.*2878_*2884del, NM_001312654.1:c.*2879_*2884del, NM_001312654.1:c.*2880_*2884del, NM_001312654.1:c.*2881_*2884del, NM_001312654.1:c.*2882_*2884del, NM_001312654.1:c.*2883_*2884del, NM_001312654.1:c.*2884del, NM_001312654.1:c.*2884dup, NM_001312654.1:c.*2883_*2884dup, NM_001312654.1:c.*2882_*2884dup, NM_001312654.1:c.*2881_*2884dup, NM_001312654.1:c.*2880_*2884dup, NM_001312654.1:c.*2879_*2884dup, NM_001312654.1:c.*2878_*2884dup, NM_001312654.1:c.*2877_*2884dup, NM_001312654.1:c.*2875_*2884dup, NM_001312654.1:c.*2873_*2884dup, NM_001312654.1:c.*2872_*2884dup, NM_001312654.1:c.*2870_*2884dup, NM_001312654.1:c.*2869_*2884dup, NM_001312654.1:c.*2868_*2884dup, NM_001312654.1:c.*2865_*2884dup, NM_001312654.1:c.*2864_*2884dup, NM_001312654.1:c.*2863_*2884dup, NM_001312654.1:c.*2862_*2884dup, NM_001312654.1:c.*2861_*2884dup, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001312654.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2868_*2884del, NM_001164178.1:c.*2870_*2884del, NM_001164178.1:c.*2871_*2884del, NM_001164178.1:c.*2872_*2884del, NM_001164178.1:c.*2873_*2884del, NM_001164178.1:c.*2874_*2884del, NM_001164178.1:c.*2875_*2884del, NM_001164178.1:c.*2876_*2884del, NM_001164178.1:c.*2877_*2884del, NM_001164178.1:c.*2878_*2884del, NM_001164178.1:c.*2879_*2884del, NM_001164178.1:c.*2880_*2884del, NM_001164178.1:c.*2881_*2884del, NM_001164178.1:c.*2882_*2884del, NM_001164178.1:c.*2883_*2884del, NM_001164178.1:c.*2884del, NM_001164178.1:c.*2884dup, NM_001164178.1:c.*2883_*2884dup, NM_001164178.1:c.*2882_*2884dup, NM_001164178.1:c.*2881_*2884dup, NM_001164178.1:c.*2880_*2884dup, NM_001164178.1:c.*2879_*2884dup, NM_001164178.1:c.*2878_*2884dup, NM_001164178.1:c.*2877_*2884dup, NM_001164178.1:c.*2875_*2884dup, NM_001164178.1:c.*2873_*2884dup, NM_001164178.1:c.*2872_*2884dup, NM_001164178.1:c.*2870_*2884dup, NM_001164178.1:c.*2869_*2884dup, NM_001164178.1:c.*2868_*2884dup, NM_001164178.1:c.*2865_*2884dup, NM_001164178.1:c.*2864_*2884dup, NM_001164178.1:c.*2863_*2884dup, NM_001164178.1:c.*2862_*2884dup, NM_001164178.1:c.*2861_*2884dup, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164178.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2868_*2884del, NM_001164181.1:c.*2870_*2884del, NM_001164181.1:c.*2871_*2884del, NM_001164181.1:c.*2872_*2884del, NM_001164181.1:c.*2873_*2884del, NM_001164181.1:c.*2874_*2884del, NM_001164181.1:c.*2875_*2884del, NM_001164181.1:c.*2876_*2884del, NM_001164181.1:c.*2877_*2884del, NM_001164181.1:c.*2878_*2884del, NM_001164181.1:c.*2879_*2884del, NM_001164181.1:c.*2880_*2884del, NM_001164181.1:c.*2881_*2884del, NM_001164181.1:c.*2882_*2884del, NM_001164181.1:c.*2883_*2884del, NM_001164181.1:c.*2884del, NM_001164181.1:c.*2884dup, NM_001164181.1:c.*2883_*2884dup, NM_001164181.1:c.*2882_*2884dup, NM_001164181.1:c.*2881_*2884dup, NM_001164181.1:c.*2880_*2884dup, NM_001164181.1:c.*2879_*2884dup, NM_001164181.1:c.*2878_*2884dup, NM_001164181.1:c.*2877_*2884dup, NM_001164181.1:c.*2875_*2884dup, NM_001164181.1:c.*2873_*2884dup, NM_001164181.1:c.*2872_*2884dup, NM_001164181.1:c.*2870_*2884dup, NM_001164181.1:c.*2869_*2884dup, NM_001164181.1:c.*2868_*2884dup, NM_001164181.1:c.*2865_*2884dup, NM_001164181.1:c.*2864_*2884dup, NM_001164181.1:c.*2863_*2884dup, NM_001164181.1:c.*2862_*2884dup, NM_001164181.1:c.*2861_*2884dup, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NM_001164181.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2868_*2884del, XM_011540371.3:c.*2870_*2884del, XM_011540371.3:c.*2871_*2884del, XM_011540371.3:c.*2872_*2884del, XM_011540371.3:c.*2873_*2884del, XM_011540371.3:c.*2874_*2884del, XM_011540371.3:c.*2875_*2884del, XM_011540371.3:c.*2876_*2884del, XM_011540371.3:c.*2877_*2884del, XM_011540371.3:c.*2878_*2884del, XM_011540371.3:c.*2879_*2884del, XM_011540371.3:c.*2880_*2884del, XM_011540371.3:c.*2881_*2884del, XM_011540371.3:c.*2882_*2884del, XM_011540371.3:c.*2883_*2884del, XM_011540371.3:c.*2884del, XM_011540371.3:c.*2884dup, XM_011540371.3:c.*2883_*2884dup, XM_011540371.3:c.*2882_*2884dup, XM_011540371.3:c.*2881_*2884dup, XM_011540371.3:c.*2880_*2884dup, XM_011540371.3:c.*2879_*2884dup, XM_011540371.3:c.*2878_*2884dup, XM_011540371.3:c.*2877_*2884dup, XM_011540371.3:c.*2875_*2884dup, XM_011540371.3:c.*2873_*2884dup, XM_011540371.3:c.*2872_*2884dup, XM_011540371.3:c.*2870_*2884dup, XM_011540371.3:c.*2869_*2884dup, XM_011540371.3:c.*2868_*2884dup, XM_011540371.3:c.*2865_*2884dup, XM_011540371.3:c.*2864_*2884dup, XM_011540371.3:c.*2863_*2884dup, XM_011540371.3:c.*2862_*2884dup, XM_011540371.3:c.*2861_*2884dup, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2868_*2884del, XM_011540371.2:c.*2870_*2884del, XM_011540371.2:c.*2871_*2884del, XM_011540371.2:c.*2872_*2884del, XM_011540371.2:c.*2873_*2884del, XM_011540371.2:c.*2874_*2884del, XM_011540371.2:c.*2875_*2884del, XM_011540371.2:c.*2876_*2884del, XM_011540371.2:c.*2877_*2884del, XM_011540371.2:c.*2878_*2884del, XM_011540371.2:c.*2879_*2884del, XM_011540371.2:c.*2880_*2884del, XM_011540371.2:c.*2881_*2884del, XM_011540371.2:c.*2882_*2884del, XM_011540371.2:c.*2883_*2884del, XM_011540371.2:c.*2884del, XM_011540371.2:c.*2884dup, XM_011540371.2:c.*2883_*2884dup, XM_011540371.2:c.*2882_*2884dup, XM_011540371.2:c.*2881_*2884dup, XM_011540371.2:c.*2880_*2884dup, XM_011540371.2:c.*2879_*2884dup, XM_011540371.2:c.*2878_*2884dup, XM_011540371.2:c.*2877_*2884dup, XM_011540371.2:c.*2875_*2884dup, XM_011540371.2:c.*2873_*2884dup, XM_011540371.2:c.*2872_*2884dup, XM_011540371.2:c.*2870_*2884dup, XM_011540371.2:c.*2869_*2884dup, XM_011540371.2:c.*2868_*2884dup, XM_011540371.2:c.*2865_*2884dup, XM_011540371.2:c.*2864_*2884dup, XM_011540371.2:c.*2863_*2884dup, XM_011540371.2:c.*2862_*2884dup, XM_011540371.2:c.*2861_*2884dup, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2868_*2884del, XM_011540371.1:c.*2870_*2884del, XM_011540371.1:c.*2871_*2884del, XM_011540371.1:c.*2872_*2884del, XM_011540371.1:c.*2873_*2884del, XM_011540371.1:c.*2874_*2884del, XM_011540371.1:c.*2875_*2884del, XM_011540371.1:c.*2876_*2884del, XM_011540371.1:c.*2877_*2884del, XM_011540371.1:c.*2878_*2884del, XM_011540371.1:c.*2879_*2884del, XM_011540371.1:c.*2880_*2884del, XM_011540371.1:c.*2881_*2884del, XM_011540371.1:c.*2882_*2884del, XM_011540371.1:c.*2883_*2884del, XM_011540371.1:c.*2884del, XM_011540371.1:c.*2884dup, XM_011540371.1:c.*2883_*2884dup, XM_011540371.1:c.*2882_*2884dup, XM_011540371.1:c.*2881_*2884dup, XM_011540371.1:c.*2880_*2884dup, XM_011540371.1:c.*2879_*2884dup, XM_011540371.1:c.*2878_*2884dup, XM_011540371.1:c.*2877_*2884dup, XM_011540371.1:c.*2875_*2884dup, XM_011540371.1:c.*2873_*2884dup, XM_011540371.1:c.*2872_*2884dup, XM_011540371.1:c.*2870_*2884dup, XM_011540371.1:c.*2869_*2884dup, XM_011540371.1:c.*2868_*2884dup, XM_011540371.1:c.*2865_*2884dup, XM_011540371.1:c.*2864_*2884dup, XM_011540371.1:c.*2863_*2884dup, XM_011540371.1:c.*2862_*2884dup, XM_011540371.1:c.*2861_*2884dup, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540371.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2868_*2884del, XM_011540370.3:c.*2870_*2884del, XM_011540370.3:c.*2871_*2884del, XM_011540370.3:c.*2872_*2884del, XM_011540370.3:c.*2873_*2884del, XM_011540370.3:c.*2874_*2884del, XM_011540370.3:c.*2875_*2884del, XM_011540370.3:c.*2876_*2884del, XM_011540370.3:c.*2877_*2884del, XM_011540370.3:c.*2878_*2884del, XM_011540370.3:c.*2879_*2884del, XM_011540370.3:c.*2880_*2884del, XM_011540370.3:c.*2881_*2884del, XM_011540370.3:c.*2882_*2884del, XM_011540370.3:c.*2883_*2884del, XM_011540370.3:c.*2884del, XM_011540370.3:c.*2884dup, XM_011540370.3:c.*2883_*2884dup, XM_011540370.3:c.*2882_*2884dup, XM_011540370.3:c.*2881_*2884dup, XM_011540370.3:c.*2880_*2884dup, XM_011540370.3:c.*2879_*2884dup, XM_011540370.3:c.*2878_*2884dup, XM_011540370.3:c.*2877_*2884dup, XM_011540370.3:c.*2875_*2884dup, XM_011540370.3:c.*2873_*2884dup, XM_011540370.3:c.*2872_*2884dup, XM_011540370.3:c.*2870_*2884dup, XM_011540370.3:c.*2869_*2884dup, XM_011540370.3:c.*2868_*2884dup, XM_011540370.3:c.*2865_*2884dup, XM_011540370.3:c.*2864_*2884dup, XM_011540370.3:c.*2863_*2884dup, XM_011540370.3:c.*2862_*2884dup, XM_011540370.3:c.*2861_*2884dup, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.3:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2868_*2884del, XM_011540370.2:c.*2870_*2884del, XM_011540370.2:c.*2871_*2884del, XM_011540370.2:c.*2872_*2884del, XM_011540370.2:c.*2873_*2884del, XM_011540370.2:c.*2874_*2884del, XM_011540370.2:c.*2875_*2884del, XM_011540370.2:c.*2876_*2884del, XM_011540370.2:c.*2877_*2884del, XM_011540370.2:c.*2878_*2884del, XM_011540370.2:c.*2879_*2884del, XM_011540370.2:c.*2880_*2884del, XM_011540370.2:c.*2881_*2884del, XM_011540370.2:c.*2882_*2884del, XM_011540370.2:c.*2883_*2884del, XM_011540370.2:c.*2884del, XM_011540370.2:c.*2884dup, XM_011540370.2:c.*2883_*2884dup, XM_011540370.2:c.*2882_*2884dup, XM_011540370.2:c.*2881_*2884dup, XM_011540370.2:c.*2880_*2884dup, XM_011540370.2:c.*2879_*2884dup, XM_011540370.2:c.*2878_*2884dup, XM_011540370.2:c.*2877_*2884dup, XM_011540370.2:c.*2875_*2884dup, XM_011540370.2:c.*2873_*2884dup, XM_011540370.2:c.*2872_*2884dup, XM_011540370.2:c.*2870_*2884dup, XM_011540370.2:c.*2869_*2884dup, XM_011540370.2:c.*2868_*2884dup, XM_011540370.2:c.*2865_*2884dup, XM_011540370.2:c.*2864_*2884dup, XM_011540370.2:c.*2863_*2884dup, XM_011540370.2:c.*2862_*2884dup, XM_011540370.2:c.*2861_*2884dup, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.2:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2868_*2884del, XM_011540370.1:c.*2870_*2884del, XM_011540370.1:c.*2871_*2884del, XM_011540370.1:c.*2872_*2884del, XM_011540370.1:c.*2873_*2884del, XM_011540370.1:c.*2874_*2884del, XM_011540370.1:c.*2875_*2884del, XM_011540370.1:c.*2876_*2884del, XM_011540370.1:c.*2877_*2884del, XM_011540370.1:c.*2878_*2884del, XM_011540370.1:c.*2879_*2884del, XM_011540370.1:c.*2880_*2884del, XM_011540370.1:c.*2881_*2884del, XM_011540370.1:c.*2882_*2884del, XM_011540370.1:c.*2883_*2884del, XM_011540370.1:c.*2884del, XM_011540370.1:c.*2884dup, XM_011540370.1:c.*2883_*2884dup, XM_011540370.1:c.*2882_*2884dup, XM_011540370.1:c.*2881_*2884dup, XM_011540370.1:c.*2880_*2884dup, XM_011540370.1:c.*2879_*2884dup, XM_011540370.1:c.*2878_*2884dup, XM_011540370.1:c.*2877_*2884dup, XM_011540370.1:c.*2875_*2884dup, XM_011540370.1:c.*2873_*2884dup, XM_011540370.1:c.*2872_*2884dup, XM_011540370.1:c.*2870_*2884dup, XM_011540370.1:c.*2869_*2884dup, XM_011540370.1:c.*2868_*2884dup, XM_011540370.1:c.*2865_*2884dup, XM_011540370.1:c.*2864_*2884dup, XM_011540370.1:c.*2863_*2884dup, XM_011540370.1:c.*2862_*2884dup, XM_011540370.1:c.*2861_*2884dup, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_011540370.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2868_*2884del, XM_047426023.1:c.*2870_*2884del, XM_047426023.1:c.*2871_*2884del, XM_047426023.1:c.*2872_*2884del, XM_047426023.1:c.*2873_*2884del, XM_047426023.1:c.*2874_*2884del, XM_047426023.1:c.*2875_*2884del, XM_047426023.1:c.*2876_*2884del, XM_047426023.1:c.*2877_*2884del, XM_047426023.1:c.*2878_*2884del, XM_047426023.1:c.*2879_*2884del, XM_047426023.1:c.*2880_*2884del, XM_047426023.1:c.*2881_*2884del, XM_047426023.1:c.*2882_*2884del, XM_047426023.1:c.*2883_*2884del, XM_047426023.1:c.*2884del, XM_047426023.1:c.*2884dup, XM_047426023.1:c.*2883_*2884dup, XM_047426023.1:c.*2882_*2884dup, XM_047426023.1:c.*2881_*2884dup, XM_047426023.1:c.*2880_*2884dup, XM_047426023.1:c.*2879_*2884dup, XM_047426023.1:c.*2878_*2884dup, XM_047426023.1:c.*2877_*2884dup, XM_047426023.1:c.*2875_*2884dup, XM_047426023.1:c.*2873_*2884dup, XM_047426023.1:c.*2872_*2884dup, XM_047426023.1:c.*2870_*2884dup, XM_047426023.1:c.*2869_*2884dup, XM_047426023.1:c.*2868_*2884dup, XM_047426023.1:c.*2865_*2884dup, XM_047426023.1:c.*2864_*2884dup, XM_047426023.1:c.*2863_*2884dup, XM_047426023.1:c.*2862_*2884dup, XM_047426023.1:c.*2861_*2884dup, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426023.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2868_*2884del, XM_047426026.1:c.*2870_*2884del, XM_047426026.1:c.*2871_*2884del, XM_047426026.1:c.*2872_*2884del, XM_047426026.1:c.*2873_*2884del, XM_047426026.1:c.*2874_*2884del, XM_047426026.1:c.*2875_*2884del, XM_047426026.1:c.*2876_*2884del, XM_047426026.1:c.*2877_*2884del, XM_047426026.1:c.*2878_*2884del, XM_047426026.1:c.*2879_*2884del, XM_047426026.1:c.*2880_*2884del, XM_047426026.1:c.*2881_*2884del, XM_047426026.1:c.*2882_*2884del, XM_047426026.1:c.*2883_*2884del, XM_047426026.1:c.*2884del, XM_047426026.1:c.*2884dup, XM_047426026.1:c.*2883_*2884dup, XM_047426026.1:c.*2882_*2884dup, XM_047426026.1:c.*2881_*2884dup, XM_047426026.1:c.*2880_*2884dup, XM_047426026.1:c.*2879_*2884dup, XM_047426026.1:c.*2878_*2884dup, XM_047426026.1:c.*2877_*2884dup, XM_047426026.1:c.*2875_*2884dup, XM_047426026.1:c.*2873_*2884dup, XM_047426026.1:c.*2872_*2884dup, XM_047426026.1:c.*2870_*2884dup, XM_047426026.1:c.*2869_*2884dup, XM_047426026.1:c.*2868_*2884dup, XM_047426026.1:c.*2865_*2884dup, XM_047426026.1:c.*2864_*2884dup, XM_047426026.1:c.*2863_*2884dup, XM_047426026.1:c.*2862_*2884dup, XM_047426026.1:c.*2861_*2884dup, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426026.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2868_*2884del, XM_047426024.1:c.*2870_*2884del, XM_047426024.1:c.*2871_*2884del, XM_047426024.1:c.*2872_*2884del, XM_047426024.1:c.*2873_*2884del, XM_047426024.1:c.*2874_*2884del, XM_047426024.1:c.*2875_*2884del, XM_047426024.1:c.*2876_*2884del, XM_047426024.1:c.*2877_*2884del, XM_047426024.1:c.*2878_*2884del, XM_047426024.1:c.*2879_*2884del, XM_047426024.1:c.*2880_*2884del, XM_047426024.1:c.*2881_*2884del, XM_047426024.1:c.*2882_*2884del, XM_047426024.1:c.*2883_*2884del, XM_047426024.1:c.*2884del, XM_047426024.1:c.*2884dup, XM_047426024.1:c.*2883_*2884dup, XM_047426024.1:c.*2882_*2884dup, XM_047426024.1:c.*2881_*2884dup, XM_047426024.1:c.*2880_*2884dup, XM_047426024.1:c.*2879_*2884dup, XM_047426024.1:c.*2878_*2884dup, XM_047426024.1:c.*2877_*2884dup, XM_047426024.1:c.*2875_*2884dup, XM_047426024.1:c.*2873_*2884dup, XM_047426024.1:c.*2872_*2884dup, XM_047426024.1:c.*2870_*2884dup, XM_047426024.1:c.*2869_*2884dup, XM_047426024.1:c.*2868_*2884dup, XM_047426024.1:c.*2865_*2884dup, XM_047426024.1:c.*2864_*2884dup, XM_047426024.1:c.*2863_*2884dup, XM_047426024.1:c.*2862_*2884dup, XM_047426024.1:c.*2861_*2884dup, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426024.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2868_*2884del, XM_047426025.1:c.*2870_*2884del, XM_047426025.1:c.*2871_*2884del, XM_047426025.1:c.*2872_*2884del, XM_047426025.1:c.*2873_*2884del, XM_047426025.1:c.*2874_*2884del, XM_047426025.1:c.*2875_*2884del, XM_047426025.1:c.*2876_*2884del, XM_047426025.1:c.*2877_*2884del, XM_047426025.1:c.*2878_*2884del, XM_047426025.1:c.*2879_*2884del, XM_047426025.1:c.*2880_*2884del, XM_047426025.1:c.*2881_*2884del, XM_047426025.1:c.*2882_*2884del, XM_047426025.1:c.*2883_*2884del, XM_047426025.1:c.*2884del, XM_047426025.1:c.*2884dup, XM_047426025.1:c.*2883_*2884dup, XM_047426025.1:c.*2882_*2884dup, XM_047426025.1:c.*2881_*2884dup, XM_047426025.1:c.*2880_*2884dup, XM_047426025.1:c.*2879_*2884dup, XM_047426025.1:c.*2878_*2884dup, XM_047426025.1:c.*2877_*2884dup, XM_047426025.1:c.*2875_*2884dup, XM_047426025.1:c.*2873_*2884dup, XM_047426025.1:c.*2872_*2884dup, XM_047426025.1:c.*2870_*2884dup, XM_047426025.1:c.*2869_*2884dup, XM_047426025.1:c.*2868_*2884dup, XM_047426025.1:c.*2865_*2884dup, XM_047426025.1:c.*2864_*2884dup, XM_047426025.1:c.*2863_*2884dup, XM_047426025.1:c.*2862_*2884dup, XM_047426025.1:c.*2861_*2884dup, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_047426025.1:c.*2884_*2885insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

    2.

    rs1491139792 [Homo sapiens]
      Variant type:
      DEL
      Alleles:
      CT>- [Show Flanks]
      Chromosome:
      10:95869241 (GRCh38)
      10:97628998 (GRCh37)
      Canonical SPDI:
      NC_000010.11:95869240:CT:
      Gene:
      ENTPD1 (Varview), ENTPD1-AS1 (Varview)
      Functional Consequence:
      3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
      Validated:
      by frequency,by alfa
      MAF:
      -=0./0 (ALFA)
      HGVS:
      NC_000010.11:g.95869241_95869242del, NC_000010.10:g.97628998_97628999del, NG_042803.1:g.162463_162464del, NM_001776.6:c.*2858_*2859del, NM_001776.5:c.*2858_*2859del, NM_001098175.2:c.*2858_*2859del, NM_001098175.1:c.*2858_*2859del, NM_001164179.2:c.*2858_*2859del, NM_001164179.1:c.*2858_*2859del, NM_001164182.2:c.*2858_*2859del, NM_001164182.1:c.*2858_*2859del, NM_001164183.2:c.*2858_*2859del, NM_001164183.1:c.*2858_*2859del, NM_001312654.1:c.*2858_*2859del, NM_001164178.1:c.*2858_*2859del, NM_001164181.1:c.*2858_*2859del, XM_011540371.3:c.*2858_*2859del, XM_011540371.2:c.*2858_*2859del, XM_011540371.1:c.*2858_*2859del, XM_011540370.3:c.*2858_*2859del, XM_011540370.2:c.*2858_*2859del, XM_011540370.1:c.*2858_*2859del, XM_047426023.1:c.*2858_*2859del, XM_047426026.1:c.*2858_*2859del, XM_047426024.1:c.*2858_*2859del, XM_047426025.1:c.*2858_*2859del

      3.

      rs1491085626 [Homo sapiens]
        Variant type:
        INS
        Alleles:
        ->G [Show Flanks]
        Chromosome:
        10:95869266 (GRCh38)
        10:97629024 (GRCh37)
        Canonical SPDI:
        NC_000010.11:95869266::G
        Gene:
        ENTPD1 (Varview), ENTPD1-AS1 (Varview)
        Functional Consequence:
        3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
        Validated:
        by frequency,by alfa,by cluster
        MAF:
        G=0./0 (ALFA)
        G=0.000054/6 (GnomAD)
        G=0.000418/7 (TOMMO)
        HGVS:
        NC_000010.11:g.95869266_95869267insG, NC_000010.10:g.97629023_97629024insG, NG_042803.1:g.162488_162489insG, NM_001776.6:c.*2883_*2884insG, NM_001776.5:c.*2883_*2884insG, NM_001098175.2:c.*2883_*2884insG, NM_001098175.1:c.*2883_*2884insG, NM_001164179.2:c.*2883_*2884insG, NM_001164179.1:c.*2883_*2884insG, NM_001164182.2:c.*2883_*2884insG, NM_001164182.1:c.*2883_*2884insG, NM_001164183.2:c.*2883_*2884insG, NM_001164183.1:c.*2883_*2884insG, NM_001312654.1:c.*2883_*2884insG, NM_001164178.1:c.*2883_*2884insG, NM_001164181.1:c.*2883_*2884insG, XM_011540371.3:c.*2883_*2884insG, XM_011540371.2:c.*2883_*2884insG, XM_011540371.1:c.*2883_*2884insG, XM_011540370.3:c.*2883_*2884insG, XM_011540370.2:c.*2883_*2884insG, XM_011540370.1:c.*2883_*2884insG, XM_047426023.1:c.*2883_*2884insG, XM_047426026.1:c.*2883_*2884insG, XM_047426024.1:c.*2883_*2884insG, XM_047426025.1:c.*2883_*2884insG

        4.

        rs1490890520 [Homo sapiens]
          Variant type:
          SNV
          Alleles:
          G>A [Show Flanks]
          Chromosome:
          10:95874024 (GRCh38)
          10:97633781 (GRCh37)
          Canonical SPDI:
          NC_000010.11:95874023:G:A
          Gene:
          ENTPD1 (Varview), ENTPD1-AS1 (Varview)
          Functional Consequence:
          3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
          Validated:
          by frequency,by alfa,by cluster
          MAF:
          A=0./0 (ALFA)
          A=0.000007/1 (GnomAD)
          A=0.000008/2 (TOPMED)
          HGVS:

          5.

          rs1490783643 [Homo sapiens]
            Variant type:
            SNV
            Alleles:
            G>C [Show Flanks]
            Chromosome:
            10:95875335 (GRCh38)
            10:97635092 (GRCh37)
            Canonical SPDI:
            NC_000010.11:95875334:G:C
            Gene:
            ENTPD1 (Varview), ENTPD1-AS1 (Varview)
            Functional Consequence:
            3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
            Validated:
            by frequency,by alfa
            MAF:
            C=0./0 (ALFA)
            C=0.000015/4 (TOPMED)
            HGVS:

            6.

            rs1490475477 [Homo sapiens]
              Variant type:
              SNV:
              Alleles:
              C>T
              Chromosome:
              no mapping
              Canonical SPDI:

              7.

              rs1490012429 has merged into rs369187001 [Homo sapiens]
                Variant type:
                DELINS
                Alleles:
                C>- [Show Flanks]
                Chromosome:
                10:95872551 (GRCh38)
                10:97632308 (GRCh37)
                Canonical SPDI:
                NC_000010.11:95872550:CC:C
                Gene:
                ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                Functional Consequence:
                genic_downstream_transcript_variant,intron_variant,3_prime_UTR_variant
                Validated:
                by frequency,by alfa,by cluster
                MAF:
                CC=0.000142/2 (ALFA)
                -=0.000086/12 (GnomAD)
                -=0.000091/24 (TOPMED)
                HGVS:

                8.

                rs1489909687 [Homo sapiens]
                  Variant type:
                  SNV
                  Alleles:
                  A>C [Show Flanks]
                  Chromosome:
                  10:95872933 (GRCh38)
                  10:97632690 (GRCh37)
                  Canonical SPDI:
                  NC_000010.11:95872932:A:C
                  Gene:
                  ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                  Functional Consequence:
                  3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                  Validated:
                  by frequency,by alfa,by cluster
                  MAF:
                  C=0./0 (ALFA)
                  C=0.000011/3 (TOPMED)
                  C=0.000021/3 (GnomAD)
                  HGVS:

                  9.

                  rs1489615824 [Homo sapiens]
                    Variant type:
                    SNV
                    Alleles:
                    G>A [Show Flanks]
                    Chromosome:
                    10:95872797 (GRCh38)
                    10:97632554 (GRCh37)
                    Canonical SPDI:
                    NC_000010.11:95872796:G:A
                    Gene:
                    ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                    Functional Consequence:
                    3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                    Validated:
                    by frequency,by alfa
                    MAF:
                    A=0.000071/1 (ALFA)
                    A=0.000011/3 (TOPMED)
                    HGVS:

                    10.

                    rs1489093144 [Homo sapiens]
                      Variant type:
                      SNV
                      Alleles:
                      T>C [Show Flanks]
                      Chromosome:
                      10:95867405 (GRCh38)
                      10:97627162 (GRCh37)
                      Canonical SPDI:
                      NC_000010.11:95867404:T:C
                      Gene:
                      ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                      Functional Consequence:
                      3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                      Validated:
                      by frequency,by cluster
                      MAF:
                      C=0.002/1 (NorthernSweden)
                      HGVS:

                      11.

                      rs1488170110 [Homo sapiens]
                        Variant type:
                        SNV
                        Alleles:
                        T>C [Show Flanks]
                        Chromosome:
                        10:95866663 (GRCh38)
                        10:97626420 (GRCh37)
                        Canonical SPDI:
                        NC_000010.11:95866662:T:C
                        Gene:
                        ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                        Functional Consequence:
                        3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                        Validated:
                        by frequency,by alfa,by cluster
                        MAF:
                        C=0./0 (ALFA)
                        C=0.000004/1 (TOPMED)
                        C=0.000007/1 (GnomAD)
                        HGVS:

                        12.

                        rs1488083390 [Homo sapiens]
                          Variant type:
                          DELINS
                          Alleles:
                          TTTA>- [Show Flanks]
                          Chromosome:
                          10:95871233 (GRCh38)
                          10:97630990 (GRCh37)
                          Canonical SPDI:
                          NC_000010.11:95871229:TTATTTA:TTA
                          Gene:
                          ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                          Functional Consequence:
                          3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
                          Validated:
                          by frequency,by alfa
                          MAF:
                          TTA=0./0 (ALFA)
                          -=0.000011/3 (TOPMED)
                          HGVS:
                          NC_000010.11:g.95871233_95871236del, NC_000010.10:g.97630990_97630993del, NG_042803.1:g.164455_164458del, NM_001776.6:c.*4850_*4853del, NM_001776.5:c.*4850_*4853del, NM_001098175.2:c.*4850_*4853del, NM_001098175.1:c.*4850_*4853del, NM_001164179.2:c.*4850_*4853del, NM_001164179.1:c.*4850_*4853del, NM_001164182.2:c.*4850_*4853del, NM_001164182.1:c.*4850_*4853del, NM_001164183.2:c.*4850_*4853del, NM_001164183.1:c.*4850_*4853del, NM_001312654.1:c.*4850_*4853del, NM_001164178.1:c.*4850_*4853del, NM_001164181.1:c.*4850_*4853del, XM_011540371.3:c.*4850_*4853del, XM_011540371.2:c.*4850_*4853del, XM_011540371.1:c.*4850_*4853del, XM_011540370.3:c.*4850_*4853del, XM_011540370.2:c.*4850_*4853del, XM_011540370.1:c.*4850_*4853del, XM_047426023.1:c.*4850_*4853del, XM_047426026.1:c.*4850_*4853del, XM_047426024.1:c.*4850_*4853del, XM_047426025.1:c.*4850_*4853del

                          13.

                          rs1487452008 [Homo sapiens]
                            Variant type:
                            SNV
                            Alleles:
                            C>A,T [Show Flanks]
                            Chromosome:
                            10:95875359 (GRCh38)
                            10:97635116 (GRCh37)
                            Canonical SPDI:
                            NC_000010.11:95875358:C:A,NC_000010.11:95875358:C:T
                            Gene:
                            ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                            Functional Consequence:
                            3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                            Validated:
                            by frequency,by alfa
                            MAF:
                            T=0./0 (ALFA)
                            A=0.000004/1 (TOPMED)
                            HGVS:
                            NC_000010.11:g.95875359C>A, NC_000010.11:g.95875359C>T, NC_000010.10:g.97635116C>A, NC_000010.10:g.97635116C>T, NG_042803.1:g.168581C>A, NG_042803.1:g.168581C>T, NM_001776.6:c.*8976C>A, NM_001776.6:c.*8976C>T, NM_001776.5:c.*8976C>A, NM_001776.5:c.*8976C>T, NM_001098175.2:c.*8976C>A, NM_001098175.2:c.*8976C>T, NM_001098175.1:c.*8976C>A, NM_001098175.1:c.*8976C>T, NM_001164179.2:c.*8976C>A, NM_001164179.2:c.*8976C>T, NM_001164179.1:c.*8976C>A, NM_001164179.1:c.*8976C>T, NM_001164182.2:c.*8976C>A, NM_001164182.2:c.*8976C>T, NM_001164182.1:c.*8976C>A, NM_001164182.1:c.*8976C>T, NM_001164183.2:c.*8976C>A, NM_001164183.2:c.*8976C>T, NM_001164183.1:c.*8976C>A, NM_001164183.1:c.*8976C>T, NM_001312654.1:c.*8976C>A, NM_001312654.1:c.*8976C>T, NM_001164178.1:c.*8976C>A, NM_001164178.1:c.*8976C>T, NM_001164181.1:c.*8976C>A, NM_001164181.1:c.*8976C>T, XM_011540371.3:c.*8976C>A, XM_011540371.3:c.*8976C>T, XM_011540371.2:c.*8976C>A, XM_011540371.2:c.*8976C>T, XM_011540371.1:c.*8976C>A, XM_011540371.1:c.*8976C>T, XM_011540370.3:c.*8976C>A, XM_011540370.3:c.*8976C>T, XM_011540370.2:c.*8976C>A, XM_011540370.2:c.*8976C>T, XM_011540370.1:c.*8976C>A, XM_011540370.1:c.*8976C>T, XM_047426023.1:c.*8976C>A, XM_047426023.1:c.*8976C>T, XM_047426026.1:c.*8976C>A, XM_047426026.1:c.*8976C>T, XM_047426024.1:c.*8976C>A, XM_047426024.1:c.*8976C>T, XM_047426025.1:c.*8976C>A, XM_047426025.1:c.*8976C>T, NM_024343.1:c.-271G>T, NM_024343.1:c.-271G>A

                            14.

                            rs1487271090 [Homo sapiens]
                              Variant type:
                              SNV
                              Alleles:
                              T>A,C [Show Flanks]
                              Chromosome:
                              10:95868554 (GRCh38)
                              10:97628311 (GRCh37)
                              Canonical SPDI:
                              NC_000010.11:95868553:T:A,NC_000010.11:95868553:T:C
                              Gene:
                              ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                              Functional Consequence:
                              3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                              Validated:
                              by frequency,by alfa
                              MAF:
                              C=0./0 (ALFA)
                              A=0.000004/1 (TOPMED)
                              HGVS:
                              NC_000010.11:g.95868554T>A, NC_000010.11:g.95868554T>C, NC_000010.10:g.97628311T>A, NC_000010.10:g.97628311T>C, NG_042803.1:g.161776T>A, NG_042803.1:g.161776T>C, NM_001776.6:c.*2171T>A, NM_001776.6:c.*2171T>C, NM_001776.5:c.*2171T>A, NM_001776.5:c.*2171T>C, NM_001098175.2:c.*2171T>A, NM_001098175.2:c.*2171T>C, NM_001098175.1:c.*2171T>A, NM_001098175.1:c.*2171T>C, NM_001164179.2:c.*2171T>A, NM_001164179.2:c.*2171T>C, NM_001164179.1:c.*2171T>A, NM_001164179.1:c.*2171T>C, NM_001164182.2:c.*2171T>A, NM_001164182.2:c.*2171T>C, NM_001164182.1:c.*2171T>A, NM_001164182.1:c.*2171T>C, NM_001164183.2:c.*2171T>A, NM_001164183.2:c.*2171T>C, NM_001164183.1:c.*2171T>A, NM_001164183.1:c.*2171T>C, NM_001312654.1:c.*2171T>A, NM_001312654.1:c.*2171T>C, NM_001164178.1:c.*2171T>A, NM_001164178.1:c.*2171T>C, NM_001164181.1:c.*2171T>A, NM_001164181.1:c.*2171T>C, XM_011540371.3:c.*2171T>A, XM_011540371.3:c.*2171T>C, XM_011540371.2:c.*2171T>A, XM_011540371.2:c.*2171T>C, XM_011540371.1:c.*2171T>A, XM_011540371.1:c.*2171T>C, XM_011540370.3:c.*2171T>A, XM_011540370.3:c.*2171T>C, XM_011540370.2:c.*2171T>A, XM_011540370.2:c.*2171T>C, XM_011540370.1:c.*2171T>A, XM_011540370.1:c.*2171T>C, XM_047426023.1:c.*2171T>A, XM_047426023.1:c.*2171T>C, XM_047426026.1:c.*2171T>A, XM_047426026.1:c.*2171T>C, XM_047426024.1:c.*2171T>A, XM_047426024.1:c.*2171T>C, XM_047426025.1:c.*2171T>A, XM_047426025.1:c.*2171T>C

                              15.

                              rs1487260923 [Homo sapiens]
                                Variant type:
                                SNV
                                Alleles:
                                C>G [Show Flanks]
                                Chromosome:
                                10:95871590 (GRCh38)
                                10:97631347 (GRCh37)
                                Canonical SPDI:
                                NC_000010.11:95871589:C:G
                                Gene:
                                ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                Functional Consequence:
                                3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                                Validated:
                                by frequency,by alfa,by cluster
                                MAF:
                                G=0./0 (ALFA)
                                G=0.000019/5 (TOPMED)
                                G=0.000036/5 (GnomAD)
                                HGVS:

                                16.

                                rs1487171411 [Homo sapiens]
                                  Variant type:
                                  SNV
                                  Alleles:
                                  C>T [Show Flanks]
                                  Chromosome:
                                  10:95874810 (GRCh38)
                                  10:97634567 (GRCh37)
                                  Canonical SPDI:
                                  NC_000010.11:95874809:C:T
                                  Gene:
                                  ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                  Functional Consequence:
                                  3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                                  Validated:
                                  by frequency,by alfa
                                  MAF:
                                  T=0.000071/1 (ALFA)
                                  T=0.000007/1 (GnomAD)
                                  HGVS:

                                  17.

                                  rs1487056923 [Homo sapiens]
                                    Variant type:
                                    SNV
                                    Alleles:
                                    C>T [Show Flanks]
                                    Chromosome:
                                    10:95873632 (GRCh38)
                                    10:97633389 (GRCh37)
                                    Canonical SPDI:
                                    NC_000010.11:95873631:C:T
                                    Gene:
                                    ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                    Functional Consequence:
                                    3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                                    Validated:
                                    by frequency,by alfa,by cluster
                                    MAF:
                                    T=0./0 (ALFA)
                                    T=0.000004/1 (TOPMED)
                                    T=0.000007/1 (GnomAD)
                                    T=0.000495/8 (TOMMO)
                                    HGVS:

                                    18.

                                    rs1486360763 [Homo sapiens]
                                      Variant type:
                                      SNV
                                      Alleles:
                                      T>C [Show Flanks]
                                      Chromosome:
                                      10:95870239 (GRCh38)
                                      10:97629996 (GRCh37)
                                      Canonical SPDI:
                                      NC_000010.11:95870238:T:C
                                      Gene:
                                      ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                      Functional Consequence:
                                      3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                                      Validated:
                                      by frequency,by alfa,by cluster
                                      MAF:
                                      C=0./0 (ALFA)
                                      C=0.000007/1 (GnomAD)
                                      C=0.000008/2 (TOPMED)
                                      HGVS:

                                      19.

                                      rs1486292575 [Homo sapiens]
                                        Variant type:
                                        SNV
                                        Alleles:
                                        G>C [Show Flanks]
                                        Chromosome:
                                        10:95867126 (GRCh38)
                                        10:97626883 (GRCh37)
                                        Canonical SPDI:
                                        NC_000010.11:95867125:G:C
                                        Gene:
                                        ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                        Functional Consequence:
                                        3_prime_UTR_variant,downstream_transcript_variant,intron_variant,genic_downstream_transcript_variant
                                        Validated:
                                        by frequency
                                        MAF:
                                        C=0.000007/1 (GnomAD)
                                        HGVS:

                                        20.

                                        rs1486164625 [Homo sapiens]
                                          Variant type:
                                          SNV
                                          Alleles:
                                          C>T [Show Flanks]
                                          Chromosome:
                                          10:95869098 (GRCh38)
                                          10:97628855 (GRCh37)
                                          Canonical SPDI:
                                          NC_000010.11:95869097:C:T
                                          Gene:
                                          ENTPD1 (Varview), ENTPD1-AS1 (Varview)
                                          Functional Consequence:
                                          3_prime_UTR_variant,intron_variant,genic_downstream_transcript_variant
                                          Validated:
                                          by frequency,by alfa,by cluster
                                          MAF:
                                          T=0./0 (ALFA)
                                          T=0.000004/1 (TOPMED)
                                          T=0.000007/1 (GnomAD)
                                          HGVS:

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