SNP Links for Gene (Select 4696) - SNP

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Select item 14912577051.

rs1491257705 [Homo sapiens]

Variant type:: SNV:
Alleles:: TG>-
Chromosome:: no mapping
Canonical SPDI:

Select item 14905079262.

rs1490507926 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:54105577 (GRCh38)
19:54608884 (GRCh37)
Canonical SPDI:: NC_000019.10:54105576:A:G
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000019.10:g.54105577A>G, NW_004166865.1:g.79944A>G, NW_003571061.2:g.79997A>G, NW_003571055.2:g.79997A>G, NC_000019.9:g.54608884A>G, NW_003571059.2:g.79997A>G, NW_003571056.2:g.79997A>G, NW_003571061.1:g.79997A>G, NW_003571057.2:g.79997A>G, NW_003571058.2:g.79997A>G, NT_187693.1:g.79997A>G, NW_003571060.1:g.79997A>G, NW_003571054.1:g.79997A>G

Select item 14904206013.

rs1490420601 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:54102304 (GRCh38)
19:54605612 (GRCh37)
Canonical SPDI:: NC_000019.10:54102303:C:T
Gene:: NDUFA3 (Varview), OSCAR (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54102304C>T, NW_004166865.1:g.76671C>T, NW_003571061.2:g.76725C>T, NW_003571055.2:g.76725C>T, NC_000019.9:g.54605612C>T, NW_003571059.2:g.76725C>T, NW_003571056.2:g.76725C>T, NW_003571061.1:g.76725C>T, NW_003571057.2:g.76725C>T, NW_003571058.2:g.76725C>T, NT_187693.1:g.76725C>T, NW_003571060.1:g.76725C>T, NW_003571054.1:g.76725C>T

Select item 14903010124.

rs1490301012 has merged into rs796770972 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 19:54105273 (GRCh38)
19:54608581 (GRCh37)
Canonical SPDI:: NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000019.10:54105264:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
HGVS:: NC_000019.10:g.54105273_54105285del, NC_000019.10:g.54105276_54105285del, NC_000019.10:g.54105277_54105285del, NC_000019.10:g.54105278_54105285del, NC_000019.10:g.54105279_54105285del, NC_000019.10:g.54105280_54105285del, NC_000019.10:g.54105281_54105285del, NC_000019.10:g.54105282_54105285del, NC_000019.10:g.54105283_54105285del, NC_000019.10:g.54105284_54105285del, NC_000019.10:g.54105285del, NC_000019.10:g.54105285dup, NC_000019.10:g.54105284_54105285dup, NC_000019.10:g.54105283_54105285dup, NC_000019.10:g.54105282_54105285dup, NC_000019.10:g.54105281_54105285dup, NC_000019.10:g.54105280_54105285dup, NC_000019.10:g.54105279_54105285dup, NC_000019.10:g.54105278_54105285dup, NC_000019.10:g.54105277_54105285dup, NC_000019.10:g.54105276_54105285dup, NC_000019.10:g.54105275_54105285dup, NC_000019.10:g.54105274_54105285dup, NC_000019.10:g.54105273_54105285dup, NC_000019.10:g.54105272_54105285dup, NC_000019.10:g.54105271_54105285dup, NC_000019.10:g.54105270_54105285dup, NC_000019.10:g.54105269_54105285dup, NC_000019.10:g.54105268_54105285dup, NC_000019.10:g.54105267_54105285dup, NC_000019.10:g.54105266_54105285dup, NC_000019.10:g.54105265_54105285dup, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.10:g.54105285_54105286insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79640_79652del, NW_004166865.1:g.79643_79652del, NW_004166865.1:g.79644_79652del, NW_004166865.1:g.79645_79652del, NW_004166865.1:g.79646_79652del, NW_004166865.1:g.79647_79652del, NW_004166865.1:g.79648_79652del, NW_004166865.1:g.79649_79652del, NW_004166865.1:g.79650_79652del, NW_004166865.1:g.79651_79652del, NW_004166865.1:g.79652del, NW_004166865.1:g.79652dup, NW_004166865.1:g.79651_79652dup, NW_004166865.1:g.79650_79652dup, NW_004166865.1:g.79649_79652dup, NW_004166865.1:g.79648_79652dup, NW_004166865.1:g.79647_79652dup, NW_004166865.1:g.79646_79652dup, NW_004166865.1:g.79645_79652dup, NW_004166865.1:g.79644_79652dup, NW_004166865.1:g.79643_79652dup, NW_004166865.1:g.79642_79652dup, NW_004166865.1:g.79641_79652dup, NW_004166865.1:g.79640_79652dup, NW_004166865.1:g.79639_79652dup, NW_004166865.1:g.79638_79652dup, NW_004166865.1:g.79637_79652dup, NW_004166865.1:g.79636_79652dup, NW_004166865.1:g.79635_79652dup, NW_004166865.1:g.79634_79652dup, NW_004166865.1:g.79633_79652dup, NW_004166865.1:g.79632_79652dup, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_004166865.1:g.79652_79653insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705dup, NW_003571061.2:g.79694_79705del, NW_003571061.2:g.79697_79705del, NW_003571061.2:g.79698_79705del, NW_003571061.2:g.79699_79705del, NW_003571061.2:g.79700_79705del, NW_003571061.2:g.79701_79705del, NW_003571061.2:g.79702_79705del, NW_003571061.2:g.79703_79705del, NW_003571061.2:g.79704_79705del, NW_003571061.2:g.79705del, NW_003571061.2:g.79704_79705dup, NW_003571061.2:g.79703_79705dup, NW_003571061.2:g.79702_79705dup, NW_003571061.2:g.79701_79705dup, NW_003571061.2:g.79700_79705dup, NW_003571061.2:g.79699_79705dup, NW_003571061.2:g.79698_79705dup, NW_003571061.2:g.79697_79705dup, NW_003571061.2:g.79696_79705dup, NW_003571061.2:g.79695_79705dup, NW_003571061.2:g.79694_79705dup, NW_003571061.2:g.79693_79705dup, NW_003571061.2:g.79692_79705dup, NW_003571061.2:g.79691_79705dup, NW_003571061.2:g.79690_79705dup, NW_003571061.2:g.79689_79705dup, NW_003571061.2:g.79688_79705dup, NW_003571061.2:g.79687_79705dup, NW_003571061.2:g.79686_79705dup, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705dup, NW_003571055.2:g.79694_79705del, NW_003571055.2:g.79697_79705del, NW_003571055.2:g.79698_79705del, NW_003571055.2:g.79699_79705del, NW_003571055.2:g.79700_79705del, NW_003571055.2:g.79701_79705del, NW_003571055.2:g.79702_79705del, NW_003571055.2:g.79703_79705del, NW_003571055.2:g.79704_79705del, NW_003571055.2:g.79705del, NW_003571055.2:g.79704_79705dup, NW_003571055.2:g.79703_79705dup, NW_003571055.2:g.79702_79705dup, NW_003571055.2:g.79701_79705dup, NW_003571055.2:g.79700_79705dup, NW_003571055.2:g.79699_79705dup, NW_003571055.2:g.79698_79705dup, NW_003571055.2:g.79697_79705dup, NW_003571055.2:g.79696_79705dup, NW_003571055.2:g.79695_79705dup, NW_003571055.2:g.79694_79705dup, NW_003571055.2:g.79693_79705dup, NW_003571055.2:g.79692_79705dup, NW_003571055.2:g.79691_79705dup, NW_003571055.2:g.79690_79705dup, NW_003571055.2:g.79689_79705dup, NW_003571055.2:g.79688_79705dup, NW_003571055.2:g.79687_79705dup, NW_003571055.2:g.79686_79705dup, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571055.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705dup, NW_003571059.2:g.79694_79705del, NW_003571059.2:g.79697_79705del, NW_003571059.2:g.79698_79705del, NW_003571059.2:g.79699_79705del, NW_003571059.2:g.79700_79705del, NW_003571059.2:g.79701_79705del, NW_003571059.2:g.79702_79705del, NW_003571059.2:g.79703_79705del, NW_003571059.2:g.79704_79705del, NW_003571059.2:g.79705del, NW_003571059.2:g.79704_79705dup, NW_003571059.2:g.79703_79705dup, NW_003571059.2:g.79702_79705dup, NW_003571059.2:g.79701_79705dup, NW_003571059.2:g.79700_79705dup, NW_003571059.2:g.79699_79705dup, NW_003571059.2:g.79698_79705dup, NW_003571059.2:g.79697_79705dup, NW_003571059.2:g.79696_79705dup, NW_003571059.2:g.79695_79705dup, NW_003571059.2:g.79694_79705dup, NW_003571059.2:g.79693_79705dup, NW_003571059.2:g.79692_79705dup, NW_003571059.2:g.79691_79705dup, NW_003571059.2:g.79690_79705dup, NW_003571059.2:g.79689_79705dup, NW_003571059.2:g.79688_79705dup, NW_003571059.2:g.79687_79705dup, NW_003571059.2:g.79686_79705dup, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571059.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705dup, NW_003571056.2:g.79694_79705del, NW_003571056.2:g.79697_79705del, NW_003571056.2:g.79698_79705del, NW_003571056.2:g.79699_79705del, NW_003571056.2:g.79700_79705del, NW_003571056.2:g.79701_79705del, NW_003571056.2:g.79702_79705del, NW_003571056.2:g.79703_79705del, NW_003571056.2:g.79704_79705del, NW_003571056.2:g.79705del, NW_003571056.2:g.79704_79705dup, NW_003571056.2:g.79703_79705dup, NW_003571056.2:g.79702_79705dup, NW_003571056.2:g.79701_79705dup, NW_003571056.2:g.79700_79705dup, NW_003571056.2:g.79699_79705dup, NW_003571056.2:g.79698_79705dup, NW_003571056.2:g.79697_79705dup, NW_003571056.2:g.79696_79705dup, NW_003571056.2:g.79695_79705dup, NW_003571056.2:g.79694_79705dup, NW_003571056.2:g.79693_79705dup, NW_003571056.2:g.79692_79705dup, NW_003571056.2:g.79691_79705dup, NW_003571056.2:g.79690_79705dup, NW_003571056.2:g.79689_79705dup, NW_003571056.2:g.79688_79705dup, NW_003571056.2:g.79687_79705dup, NW_003571056.2:g.79686_79705dup, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571056.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705dup, NW_003571057.2:g.79694_79705del, NW_003571057.2:g.79697_79705del, NW_003571057.2:g.79698_79705del, NW_003571057.2:g.79699_79705del, NW_003571057.2:g.79700_79705del, NW_003571057.2:g.79701_79705del, NW_003571057.2:g.79702_79705del, NW_003571057.2:g.79703_79705del, NW_003571057.2:g.79704_79705del, NW_003571057.2:g.79705del, NW_003571057.2:g.79704_79705dup, NW_003571057.2:g.79703_79705dup, NW_003571057.2:g.79702_79705dup, NW_003571057.2:g.79701_79705dup, NW_003571057.2:g.79700_79705dup, NW_003571057.2:g.79699_79705dup, NW_003571057.2:g.79698_79705dup, NW_003571057.2:g.79697_79705dup, NW_003571057.2:g.79696_79705dup, NW_003571057.2:g.79695_79705dup, NW_003571057.2:g.79694_79705dup, NW_003571057.2:g.79693_79705dup, NW_003571057.2:g.79692_79705dup, NW_003571057.2:g.79691_79705dup, NW_003571057.2:g.79690_79705dup, NW_003571057.2:g.79689_79705dup, NW_003571057.2:g.79688_79705dup, NW_003571057.2:g.79687_79705dup, NW_003571057.2:g.79686_79705dup, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571057.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705dup, NW_003571058.2:g.79694_79705del, NW_003571058.2:g.79697_79705del, NW_003571058.2:g.79698_79705del, NW_003571058.2:g.79699_79705del, NW_003571058.2:g.79700_79705del, NW_003571058.2:g.79701_79705del, NW_003571058.2:g.79702_79705del, NW_003571058.2:g.79703_79705del, NW_003571058.2:g.79704_79705del, NW_003571058.2:g.79705del, NW_003571058.2:g.79704_79705dup, NW_003571058.2:g.79703_79705dup, NW_003571058.2:g.79702_79705dup, NW_003571058.2:g.79701_79705dup, NW_003571058.2:g.79700_79705dup, NW_003571058.2:g.79699_79705dup, NW_003571058.2:g.79698_79705dup, NW_003571058.2:g.79697_79705dup, NW_003571058.2:g.79696_79705dup, NW_003571058.2:g.79695_79705dup, NW_003571058.2:g.79694_79705dup, NW_003571058.2:g.79693_79705dup, NW_003571058.2:g.79692_79705dup, NW_003571058.2:g.79691_79705dup, NW_003571058.2:g.79690_79705dup, NW_003571058.2:g.79689_79705dup, NW_003571058.2:g.79688_79705dup, NW_003571058.2:g.79687_79705dup, NW_003571058.2:g.79686_79705dup, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571058.2:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705dup, NT_187693.1:g.79694_79705del, NT_187693.1:g.79697_79705del, NT_187693.1:g.79698_79705del, NT_187693.1:g.79699_79705del, NT_187693.1:g.79700_79705del, NT_187693.1:g.79701_79705del, NT_187693.1:g.79702_79705del, NT_187693.1:g.79703_79705del, NT_187693.1:g.79704_79705del, NT_187693.1:g.79705del, NT_187693.1:g.79704_79705dup, NT_187693.1:g.79703_79705dup, NT_187693.1:g.79702_79705dup, NT_187693.1:g.79701_79705dup, NT_187693.1:g.79700_79705dup, NT_187693.1:g.79699_79705dup, NT_187693.1:g.79698_79705dup, NT_187693.1:g.79697_79705dup, NT_187693.1:g.79696_79705dup, NT_187693.1:g.79695_79705dup, NT_187693.1:g.79694_79705dup, NT_187693.1:g.79693_79705dup, NT_187693.1:g.79692_79705dup, NT_187693.1:g.79691_79705dup, NT_187693.1:g.79690_79705dup, NT_187693.1:g.79689_79705dup, NT_187693.1:g.79688_79705dup, NT_187693.1:g.79687_79705dup, NT_187693.1:g.79686_79705dup, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187693.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705dup, NW_003571060.1:g.79694_79705del, NW_003571060.1:g.79697_79705del, NW_003571060.1:g.79698_79705del, NW_003571060.1:g.79699_79705del, NW_003571060.1:g.79700_79705del, NW_003571060.1:g.79701_79705del, NW_003571060.1:g.79702_79705del, NW_003571060.1:g.79703_79705del, NW_003571060.1:g.79704_79705del, NW_003571060.1:g.79705del, NW_003571060.1:g.79704_79705dup, NW_003571060.1:g.79703_79705dup, NW_003571060.1:g.79702_79705dup, NW_003571060.1:g.79701_79705dup, NW_003571060.1:g.79700_79705dup, NW_003571060.1:g.79699_79705dup, NW_003571060.1:g.79698_79705dup, NW_003571060.1:g.79697_79705dup, NW_003571060.1:g.79696_79705dup, NW_003571060.1:g.79695_79705dup, NW_003571060.1:g.79694_79705dup, NW_003571060.1:g.79693_79705dup, NW_003571060.1:g.79692_79705dup, NW_003571060.1:g.79691_79705dup, NW_003571060.1:g.79690_79705dup, NW_003571060.1:g.79689_79705dup, NW_003571060.1:g.79688_79705dup, NW_003571060.1:g.79687_79705dup, NW_003571060.1:g.79686_79705dup, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571060.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705dup, NW_003571054.1:g.79694_79705del, NW_003571054.1:g.79697_79705del, NW_003571054.1:g.79698_79705del, NW_003571054.1:g.79699_79705del, NW_003571054.1:g.79700_79705del, NW_003571054.1:g.79701_79705del, NW_003571054.1:g.79702_79705del, NW_003571054.1:g.79703_79705del, NW_003571054.1:g.79704_79705del, NW_003571054.1:g.79705del, NW_003571054.1:g.79704_79705dup, NW_003571054.1:g.79703_79705dup, NW_003571054.1:g.79702_79705dup, NW_003571054.1:g.79701_79705dup, NW_003571054.1:g.79700_79705dup, NW_003571054.1:g.79699_79705dup, NW_003571054.1:g.79698_79705dup, NW_003571054.1:g.79697_79705dup, NW_003571054.1:g.79696_79705dup, NW_003571054.1:g.79695_79705dup, NW_003571054.1:g.79694_79705dup, NW_003571054.1:g.79693_79705dup, NW_003571054.1:g.79692_79705dup, NW_003571054.1:g.79691_79705dup, NW_003571054.1:g.79690_79705dup, NW_003571054.1:g.79689_79705dup, NW_003571054.1:g.79688_79705dup, NW_003571054.1:g.79687_79705dup, NW_003571054.1:g.79686_79705dup, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571054.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592dup, NC_000019.9:g.54608581_54608592del, NC_000019.9:g.54608584_54608592del, NC_000019.9:g.54608585_54608592del, NC_000019.9:g.54608586_54608592del, NC_000019.9:g.54608587_54608592del, NC_000019.9:g.54608588_54608592del, NC_000019.9:g.54608589_54608592del, NC_000019.9:g.54608590_54608592del, NC_000019.9:g.54608591_54608592del, NC_000019.9:g.54608592del, NC_000019.9:g.54608591_54608592dup, NC_000019.9:g.54608590_54608592dup, NC_000019.9:g.54608589_54608592dup, NC_000019.9:g.54608588_54608592dup, NC_000019.9:g.54608587_54608592dup, NC_000019.9:g.54608586_54608592dup, NC_000019.9:g.54608585_54608592dup, NC_000019.9:g.54608584_54608592dup, NC_000019.9:g.54608583_54608592dup, NC_000019.9:g.54608582_54608592dup, NC_000019.9:g.54608581_54608592dup, NC_000019.9:g.54608580_54608592dup, NC_000019.9:g.54608579_54608592dup, NC_000019.9:g.54608578_54608592dup, NC_000019.9:g.54608577_54608592dup, NC_000019.9:g.54608576_54608592dup, NC_000019.9:g.54608575_54608592dup, NC_000019.9:g.54608574_54608592dup, NC_000019.9:g.54608573_54608592dup, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000019.9:g.54608592_54608593insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705dup, NW_003571061.1:g.79694_79705del, NW_003571061.1:g.79697_79705del, NW_003571061.1:g.79698_79705del, NW_003571061.1:g.79699_79705del, NW_003571061.1:g.79700_79705del, NW_003571061.1:g.79701_79705del, NW_003571061.1:g.79702_79705del, NW_003571061.1:g.79703_79705del, NW_003571061.1:g.79704_79705del, NW_003571061.1:g.79705del, NW_003571061.1:g.79704_79705dup, NW_003571061.1:g.79703_79705dup, NW_003571061.1:g.79702_79705dup, NW_003571061.1:g.79701_79705dup, NW_003571061.1:g.79700_79705dup, NW_003571061.1:g.79699_79705dup, NW_003571061.1:g.79698_79705dup, NW_003571061.1:g.79697_79705dup, NW_003571061.1:g.79696_79705dup, NW_003571061.1:g.79695_79705dup, NW_003571061.1:g.79694_79705dup, NW_003571061.1:g.79693_79705dup, NW_003571061.1:g.79692_79705dup, NW_003571061.1:g.79691_79705dup, NW_003571061.1:g.79690_79705dup, NW_003571061.1:g.79689_79705dup, NW_003571061.1:g.79688_79705dup, NW_003571061.1:g.79687_79705dup, NW_003571061.1:g.79686_79705dup, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NW_003571061.1:g.79705_79706insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14902502525.

rs1490250252 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:54104586 (GRCh38)
19:54607894 (GRCh37)
Canonical SPDI:: NC_000019.10:54104585:C:T
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000071/2 (TOMMO)
HGVS:: NC_000019.10:g.54104586C>T, NW_004166865.1:g.78953C>T, NW_003571061.2:g.79007C>T, NW_003571055.2:g.79007C>T, NC_000019.9:g.54607894C>T, NW_003571059.2:g.79007C>T, NW_003571056.2:g.79007C>T, NW_003571061.1:g.79007C>T, NW_003571057.2:g.79007C>T, NW_003571058.2:g.79007C>T, NT_187693.1:g.79007C>T, NW_003571060.1:g.79007C>T, NW_003571054.1:g.79007C>T

Select item 14897508916.

rs1489750891 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:54104688 (GRCh38)
19:54607996 (GRCh37)
Canonical SPDI:: NC_000019.10:54104687:T:C
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000064/17 (TOPMED)
C=0.000093/13 (GnomAD)
C=0.000156/1 (1000Genomes)
HGVS:: NC_000019.10:g.54104688T>C, NW_004166865.1:g.79055T>C, NW_003571061.2:g.79109T>C, NW_003571055.2:g.79109T>C, NC_000019.9:g.54607996T>C, NW_003571059.2:g.79109T>C, NW_003571056.2:g.79109T>C, NW_003571061.1:g.79109T>C, NW_003571057.2:g.79109T>C, NW_003571058.2:g.79109T>C, NT_187693.1:g.79109T>C, NW_003571060.1:g.79109T>C, NW_003571054.1:g.79109T>C

Select item 14893993737.

rs1489399373 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:54103207 (GRCh38)
19:54606515 (GRCh37)
Canonical SPDI:: NC_000019.10:54103206:C:A
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.54103207C>A, NW_004166865.1:g.77574C>A, NW_003571061.2:g.77628C>A, NW_003571055.2:g.77628C>A, NC_000019.9:g.54606515C>A, NW_003571059.2:g.77628C>A, NW_003571056.2:g.77628C>A, NW_003571061.1:g.77628C>A, NW_003571057.2:g.77628C>A, NW_003571058.2:g.77628C>A, NT_187693.1:g.77628C>A, NW_003571060.1:g.77628C>A, NW_003571054.1:g.77628C>A

Select item 14893527528.

rs1489352752 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:54102217 (GRCh38)
19:54605525 (GRCh37)
Canonical SPDI:: NC_000019.10:54102216:A:G
Gene:: NDUFA3 (Varview), OSCAR (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.54102217A>G, NW_004166865.1:g.76584A>G, NW_003571061.2:g.76638A>G, NW_003571055.2:g.76638A>G, NC_000019.9:g.54605525A>G, NW_003571059.2:g.76638A>G, NW_003571056.2:g.76638A>G, NW_003571061.1:g.76638A>G, NW_003571057.2:g.76638A>G, NW_003571058.2:g.76638A>G, NT_187693.1:g.76638A>G, NW_003571060.1:g.76638A>G, NW_003571054.1:g.76638A>G

Select item 14884072299.

rs1488407229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:54106752 (GRCh38)
19:54610059 (GRCh37)
Canonical SPDI:: NC_000019.10:54106751:T:C
Gene:: NDUFA3 (Varview), TFPT (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54106752T>C, NW_004166865.1:g.81119T>C, NW_003571061.2:g.81172T>C, NW_003571055.2:g.81172T>C, NC_000019.9:g.54610059T>C, NW_003571059.2:g.81172T>C, NW_003571056.2:g.81172T>C, NW_003571061.1:g.81172T>C, NW_003571057.2:g.81172T>C, NW_003571058.2:g.81172T>C, NT_187693.1:g.81172T>C, NW_003571060.1:g.81172T>C, NW_003571054.1:g.81172T>C

Select item 148823125010.

rs1488231250 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:54103814 (GRCh38)
19:54607122 (GRCh37)
Canonical SPDI:: NC_000019.10:54103813:G:A
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54103814G>A, NW_004166865.1:g.78181G>A, NW_003571061.2:g.78235G>A, NW_003571055.2:g.78235G>A, NC_000019.9:g.54607122G>A, NW_003571059.2:g.78235G>A, NW_003571056.2:g.78235G>A, NW_003571061.1:g.78235G>A, NW_003571057.2:g.78235G>A, NW_003571058.2:g.78235G>A, NT_187693.1:g.78235G>A, NW_003571060.1:g.78235G>A, NW_003571054.1:g.78235G>A

Select item 148809955511.

rs1488099555 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:54102964 (GRCh38)
19:54606272 (GRCh37)
Canonical SPDI:: NC_000019.10:54102963:G:A
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.54102964G>A, NW_004166865.1:g.77331G>A, NW_003571061.2:g.77385G>A, NW_003571055.2:g.77385G>A, NC_000019.9:g.54606272G>A, NW_003571059.2:g.77385G>A, NW_003571056.2:g.77385G>A, NW_003571061.1:g.77385G>A, NW_003571057.2:g.77385G>A, NW_003571058.2:g.77385G>A, NT_187693.1:g.77385G>A, NW_003571060.1:g.77385G>A, NW_003571054.1:g.77385G>A

Select item 148798152512.

rs1487981525 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 19:54102496 (GRCh38)
19:54605804 (GRCh37)
Canonical SPDI:: NC_000019.10:54102495:T:A,NC_000019.10:54102495:T:C
Gene:: NDUFA3 (Varview), OSCAR (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00003/8 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000019.10:g.54102496T>A, NC_000019.10:g.54102496T>C, NW_004166865.1:g.76863T>A, NW_004166865.1:g.76863T>C, NW_003571061.2:g.76917T>A, NW_003571061.2:g.76917T>C, NW_003571055.2:g.76917T>A, NW_003571055.2:g.76917T>C, NC_000019.9:g.54605804T>A, NC_000019.9:g.54605804T>C, NW_003571059.2:g.76917T>A, NW_003571059.2:g.76917T>C, NW_003571056.2:g.76917T>A, NW_003571056.2:g.76917T>C, NW_003571061.1:g.76917T>A, NW_003571061.1:g.76917T>C, NW_003571057.2:g.76917T>A, NW_003571057.2:g.76917T>C, NW_003571058.2:g.76917T>A, NW_003571058.2:g.76917T>C, NT_187693.1:g.76917T>A, NT_187693.1:g.76917T>C, NW_003571060.1:g.76917T>A, NW_003571060.1:g.76917T>C, NW_003571054.1:g.76917T>A, NW_003571054.1:g.76917T>C

Select item 148797355513.

rs1487973555 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:54100459 (GRCh38)
19:54603750 (GRCh37)
Canonical SPDI:: NC_000019.10:54100458:A:T
Gene:: OSCAR (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.54100459A>T, NW_004166865.1:g.74826A>T, NW_003571061.2:g.74863A>T, NW_003571055.2:g.74863A>T, NC_000019.9:g.54603750A>T, NW_003571059.2:g.74863A>T, NW_003571056.2:g.74863A>T, NW_003571061.1:g.74863A>T, NW_003571057.2:g.74863A>T, NW_003571058.2:g.74863A>T, NT_187693.1:g.74863A>T, NW_003571060.1:g.74863A>T, NW_003571054.1:g.74863A>T

Select item 148776616714.

rs1487766167 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:54103522 (GRCh38)
19:54606830 (GRCh37)
Canonical SPDI:: NC_000019.10:54103521:G:A
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.54103522G>A, NW_004166865.1:g.77889G>A, NW_003571061.2:g.77943G>A, NW_003571055.2:g.77943G>A, NC_000019.9:g.54606830G>A, NW_003571059.2:g.77943G>A, NW_003571056.2:g.77943G>A, NW_003571061.1:g.77943G>A, NW_003571057.2:g.77943G>A, NW_003571058.2:g.77943G>A, NT_187693.1:g.77943G>A, NW_003571060.1:g.77943G>A, NW_003571054.1:g.77943G>A

Select item 148771542115.

rs1487715421 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:54102642 (GRCh38)
19:54605950 (GRCh37)
Canonical SPDI:: NC_000019.10:54102641:C:T
Gene:: NDUFA3 (Varview), OSCAR (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.54102642C>T, NW_004166865.1:g.77009C>T, NW_003571061.2:g.77063C>T, NW_003571055.2:g.77063C>T, NC_000019.9:g.54605950C>T, NW_003571059.2:g.77063C>T, NW_003571056.2:g.77063C>T, NW_003571061.1:g.77063C>T, NW_003571057.2:g.77063C>T, NW_003571058.2:g.77063C>T, NT_187693.1:g.77063C>T, NW_003571060.1:g.77063C>T, NW_003571054.1:g.77063C>T

Select item 148767923216.

rs1487679232 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:54103424 (GRCh38)
19:54606732 (GRCh37)
Canonical SPDI:: NC_000019.10:54103423:C:G
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000019.10:g.54103424C>G, NW_004166865.1:g.77791C>G, NW_003571061.2:g.77845C>G, NW_003571055.2:g.77845C>G, NC_000019.9:g.54606732C>G, NW_003571059.2:g.77845C>G, NW_003571056.2:g.77845C>G, NW_003571061.1:g.77845C>G, NW_003571057.2:g.77845C>G, NW_003571058.2:g.77845C>G, NT_187693.1:g.77845C>G, NW_003571060.1:g.77845C>G, NW_003571054.1:g.77845C>G

Select item 148743307217.

rs1487433072 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:54103905 (GRCh38)
19:54607213 (GRCh37)
Canonical SPDI:: NC_000019.10:54103904:T:C
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000084/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54103905T>C, NW_004166865.1:g.78272T>C, NW_003571061.2:g.78326T>C, NW_003571055.2:g.78326T>C, NC_000019.9:g.54607213T>C, NW_003571059.2:g.78326T>C, NW_003571056.2:g.78326T>C, NW_003571061.1:g.78326T>C, NW_003571057.2:g.78326T>C, NW_003571058.2:g.78326T>C, NT_187693.1:g.78326T>C, NW_003571060.1:g.78326T>C, NW_003571054.1:g.78326T>C

Select item 148708075318.

rs1487080753 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:54103925 (GRCh38)
19:54607233 (GRCh37)
Canonical SPDI:: NC_000019.10:54103924:C:G
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.54103925C>G, NW_004166865.1:g.78292C>G, NW_003571061.2:g.78346C>G, NW_003571055.2:g.78346C>G, NC_000019.9:g.54607233C>G, NW_003571059.2:g.78346C>G, NW_003571056.2:g.78346C>G, NW_003571061.1:g.78346C>G, NW_003571057.2:g.78346C>G, NW_003571058.2:g.78346C>G, NT_187693.1:g.78346C>G, NW_003571060.1:g.78346C>G, NW_003571054.1:g.78346C>G

Select item 148705129619.

rs1487051296 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:54104698 (GRCh38)
19:54608006 (GRCh37)
Canonical SPDI:: NC_000019.10:54104697:A:G
Gene:: NDUFA3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54104698A>G, NW_004166865.1:g.79065A>G, NW_003571061.2:g.79119A>G, NW_003571055.2:g.79119A>G, NC_000019.9:g.54608006A>G, NW_003571059.2:g.79119A>G, NW_003571056.2:g.79119A>G, NW_003571061.1:g.79119A>G, NW_003571057.2:g.79119A>G, NW_003571058.2:g.79119A>G, NT_187693.1:g.79119A>G, NW_003571060.1:g.79119A>G, NW_003571054.1:g.79119A>G

Select item 148684587920.

rs1486845879 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:54107379 (GRCh38)
19:54610686 (GRCh37)
Canonical SPDI:: NC_000019.10:54107378:G:A
Gene:: NDUFA3 (Varview), TFPT (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.54107379G>A, NW_004166865.1:g.81746G>A, NW_003571061.2:g.81799G>A, NW_003571055.2:g.81799G>A, NC_000019.9:g.54610686G>A, NW_003571059.2:g.81799G>A, NW_003571056.2:g.81799G>A, NW_003571061.1:g.81799G>A, NW_003571057.2:g.81799G>A, NW_003571058.2:g.81799G>A, NT_187693.1:g.81799G>A, NW_003571060.1:g.81799G>A, NW_003571054.1:g.81799G>A, NM_004542.4:c.*477G>A

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