SNP Links for Nucleotide (Select 635172888) - SNP

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Select item 14915836161.

rs1491583616 has merged into rs757107375 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:75773449 (GRCh38)
1:76239134 (GRCh37)
Canonical SPDI:: NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75773440:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.5/20 (GENOME_DK)
HGVS:: NC_000001.11:g.75773449_75773462del, NC_000001.11:g.75773450_75773462del, NC_000001.11:g.75773453_75773462del, NC_000001.11:g.75773454_75773462del, NC_000001.11:g.75773455_75773462del, NC_000001.11:g.75773456_75773462del, NC_000001.11:g.75773457_75773462del, NC_000001.11:g.75773458_75773462del, NC_000001.11:g.75773459_75773462del, NC_000001.11:g.75773460_75773462del, NC_000001.11:g.75773461_75773462del, NC_000001.11:g.75773462del, NC_000001.11:g.75773462dup, NC_000001.11:g.75773461_75773462dup, NC_000001.11:g.75773460_75773462dup, NC_000001.11:g.75773459_75773462dup, NC_000001.11:g.75773458_75773462dup, NC_000001.11:g.75773457_75773462dup, NC_000001.11:g.75773456_75773462dup, NC_000001.11:g.75773449_75773462dup, NC_000001.11:g.75773448_75773462dup, NC_000001.11:g.75773447_75773462dup, NC_000001.11:g.75773446_75773462dup, NC_000001.11:g.75773445_75773462dup, NC_000001.10:g.76239134_76239147del, NC_000001.10:g.76239135_76239147del, NC_000001.10:g.76239138_76239147del, NC_000001.10:g.76239139_76239147del, NC_000001.10:g.76239140_76239147del, NC_000001.10:g.76239141_76239147del, NC_000001.10:g.76239142_76239147del, NC_000001.10:g.76239143_76239147del, NC_000001.10:g.76239144_76239147del, NC_000001.10:g.76239145_76239147del, NC_000001.10:g.76239146_76239147del, NC_000001.10:g.76239147del, NC_000001.10:g.76239147dup, NC_000001.10:g.76239146_76239147dup, NC_000001.10:g.76239145_76239147dup, NC_000001.10:g.76239144_76239147dup, NC_000001.10:g.76239143_76239147dup, NC_000001.10:g.76239142_76239147dup, NC_000001.10:g.76239141_76239147dup, NC_000001.10:g.76239134_76239147dup, NC_000001.10:g.76239133_76239147dup, NC_000001.10:g.76239132_76239147dup, NC_000001.10:g.76239131_76239147dup, NC_000001.10:g.76239130_76239147dup, NG_007045.2:g.54092_54105del, NG_007045.2:g.54093_54105del, NG_007045.2:g.54096_54105del, NG_007045.2:g.54097_54105del, NG_007045.2:g.54098_54105del, NG_007045.2:g.54099_54105del, NG_007045.2:g.54100_54105del, NG_007045.2:g.54101_54105del, NG_007045.2:g.54102_54105del, NG_007045.2:g.54103_54105del, NG_007045.2:g.54104_54105del, NG_007045.2:g.54105del, NG_007045.2:g.54105dup, NG_007045.2:g.54104_54105dup, NG_007045.2:g.54103_54105dup, NG_007045.2:g.54102_54105dup, NG_007045.2:g.54101_54105dup, NG_007045.2:g.54100_54105dup, NG_007045.2:g.54099_54105dup, NG_007045.2:g.54092_54105dup, NG_007045.2:g.54091_54105dup, NG_007045.2:g.54090_54105dup, NG_007045.2:g.54089_54105dup, NG_007045.2:g.54088_54105dup

Select item 14915824782.

rs1491582478 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:75735319 (GRCh38)
1:76201004 (GRCh37)
Canonical SPDI:: NC_000001.11:75735318:CA:
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00506/60 (ALFA)
HGVS:: NC_000001.11:g.75735319_75735320del, NC_000001.10:g.76201004_76201005del, NG_007045.2:g.15962_15963del

Select item 14915742123.

rs1491574212 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:75737327 (GRCh38)
1:76203012 (GRCh37)
Canonical SPDI:: NC_000001.11:75737326:TG:
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.00234/39 (TOMMO)
-=0.00274/5 (Korea1K)
HGVS:: NC_000001.11:g.75737327_75737328del, NC_000001.10:g.76203012_76203013del, NG_007045.2:g.17970_17971del

Select item 14915724714.

rs1491572471 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:75766880 (GRCh38)
1:76232566 (GRCh37)
Canonical SPDI:: NC_000001.11:75766880::T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.75766880_75766881insT, NC_000001.10:g.76232565_76232566insT, NG_007045.2:g.47523_47524insT

Select item 14915374275.

rs1491537427 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>-,CACA,CACACA [Show Flanks]
Chromosome:: 1:75737277 (GRCh38)
1:76202962 (GRCh37)
Canonical SPDI:: NC_000001.11:75737264:CACACACACACACA:CACACACACACA,NC_000001.11:75737264:CACACACACACACA:CACACACACACACACA,NC_000001.11:75737264:CACACACACACACA:CACACACACACACACACA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CACACACACACACACA=0./0 (ALFA)
-=0.00002/2 (GnomAD)
HGVS:: NC_000001.11:g.75737265CA[6], NC_000001.11:g.75737265CA[8], NC_000001.11:g.75737265CA[9], NC_000001.10:g.76202950CA[6], NC_000001.10:g.76202950CA[8], NC_000001.10:g.76202950CA[9], NG_007045.2:g.17908CA[6], NG_007045.2:g.17908CA[8], NG_007045.2:g.17908CA[9]

Select item 14913574616.

rs1491357461 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:75766881 (GRCh38)
1:76232566 (GRCh37)
Canonical SPDI:: NC_000001.11:75766879:AGA:A
Validated:: by frequency
MAF:: -=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.75766881_75766882del, NC_000001.10:g.76232566_76232567del, NG_007045.2:g.47524_47525del

Select item 14913294427.

rs1491329442 has merged into rs368688785 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATATATATATATATATATATATATATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT,ATATATATATATATATATATATAT,ATATATATATATATATATATATATAT,ATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATAT,ATATATATATATATATATATATATATATATATATATATATATATATATATATATAT [Show Flanks]
Chromosome:: 1:75737288 (GRCh38)
1:76202973 (GRCh37)
Canonical SPDI:: NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT,NC_000001.11:75737279:ATATATATATATATATATATATATATATATATATATATATATATATAT:ATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAT
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATAT=0./0 (ALFA)
HGVS:: NC_000001.11:g.75737280AT[4], NC_000001.11:g.75737280AT[5], NC_000001.11:g.75737280AT[6], NC_000001.11:g.75737280AT[7], NC_000001.11:g.75737280AT[8], NC_000001.11:g.75737280AT[9], NC_000001.11:g.75737280AT[10], NC_000001.11:g.75737280AT[11], NC_000001.11:g.75737280AT[12], NC_000001.11:g.75737280AT[13], NC_000001.11:g.75737280AT[14], NC_000001.11:g.75737280AT[15], NC_000001.11:g.75737280AT[16], NC_000001.11:g.75737280AT[17], NC_000001.11:g.75737280AT[18], NC_000001.11:g.75737280AT[19], NC_000001.11:g.75737280AT[20], NC_000001.11:g.75737280AT[21], NC_000001.11:g.75737280AT[22], NC_000001.11:g.75737280AT[23], NC_000001.11:g.75737280AT[25], NC_000001.11:g.75737280AT[26], NC_000001.11:g.75737280AT[27], NC_000001.11:g.75737280AT[28], NC_000001.11:g.75737280AT[29], NC_000001.11:g.75737280AT[30], NC_000001.11:g.75737280AT[31], NC_000001.11:g.75737280AT[32], NC_000001.10:g.76202965AT[4], NC_000001.10:g.76202965AT[5], NC_000001.10:g.76202965AT[6], NC_000001.10:g.76202965AT[7], NC_000001.10:g.76202965AT[8], NC_000001.10:g.76202965AT[9], NC_000001.10:g.76202965AT[10], NC_000001.10:g.76202965AT[11], NC_000001.10:g.76202965AT[12], NC_000001.10:g.76202965AT[13], NC_000001.10:g.76202965AT[14], NC_000001.10:g.76202965AT[15], NC_000001.10:g.76202965AT[16], NC_000001.10:g.76202965AT[17], NC_000001.10:g.76202965AT[18], NC_000001.10:g.76202965AT[19], NC_000001.10:g.76202965AT[20], NC_000001.10:g.76202965AT[21], NC_000001.10:g.76202965AT[22], NC_000001.10:g.76202965AT[23], NC_000001.10:g.76202965AT[25], NC_000001.10:g.76202965AT[26], NC_000001.10:g.76202965AT[27], NC_000001.10:g.76202965AT[28], NC_000001.10:g.76202965AT[29], NC_000001.10:g.76202965AT[30], NC_000001.10:g.76202965AT[31], NC_000001.10:g.76202965AT[32], NG_007045.2:g.17923AT[4], NG_007045.2:g.17923AT[5], NG_007045.2:g.17923AT[6], NG_007045.2:g.17923AT[7], NG_007045.2:g.17923AT[8], NG_007045.2:g.17923AT[9], NG_007045.2:g.17923AT[10], NG_007045.2:g.17923AT[11], NG_007045.2:g.17923AT[12], NG_007045.2:g.17923AT[13], NG_007045.2:g.17923AT[14], NG_007045.2:g.17923AT[15], NG_007045.2:g.17923AT[16], NG_007045.2:g.17923AT[17], NG_007045.2:g.17923AT[18], NG_007045.2:g.17923AT[19], NG_007045.2:g.17923AT[20], NG_007045.2:g.17923AT[21], NG_007045.2:g.17923AT[22], NG_007045.2:g.17923AT[23], NG_007045.2:g.17923AT[25], NG_007045.2:g.17923AT[26], NG_007045.2:g.17923AT[27], NG_007045.2:g.17923AT[28], NG_007045.2:g.17923AT[29], NG_007045.2:g.17923AT[30], NG_007045.2:g.17923AT[31], NG_007045.2:g.17923AT[32]

Select item 14913096558.

rs1491309655 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T,TATATATGT,TTT [Show Flanks]
Chromosome:: 1:75737280 (GRCh38)
1:76202966 (GRCh37)
Canonical SPDI:: NC_000001.11:75737280:T:TT,NC_000001.11:75737280:T:TTATATATGT,NC_000001.11:75737280:T:TTTT
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTATATATGT=0./0 (ALFA)
HGVS:: NC_000001.11:g.75737281dup, NC_000001.11:g.75737281_75737282insTATATATGT, NC_000001.11:g.75737281_75737282insTTT, NC_000001.10:g.76202966dup, NC_000001.10:g.76202966_76202967insTATATATGT, NC_000001.10:g.76202966_76202967insTTT, NG_007045.2:g.17924dup, NG_007045.2:g.17924_17925insTATATATGT, NG_007045.2:g.17924_17925insTTT

Select item 14912669169.

rs1491266916 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AA [Show Flanks]
Chromosome:: 1:75737265 (GRCh38)
1:76202951 (GRCh37)
Canonical SPDI:: NC_000001.11:75737265:A:AAA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AAA=0./0 (ALFA)
HGVS:: NC_000001.11:g.75737266_75737267insAA, NC_000001.10:g.76202951_76202952insAA, NG_007045.2:g.17909_17910insAA

Select item 149124468410.

rs1491244684 has merged into rs573854152 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,TTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 1:75758061 (GRCh38)
1:76223746 (GRCh37)
Canonical SPDI:: NC_000001.11:75758055:TTTTTTTTT:TTTTT,NC_000001.11:75758055:TTTTTTTTT:TTTTTTTT,NC_000001.11:75758055:TTTTTTTTT:TTTTTTTTTT,NC_000001.11:75758055:TTTTTTTTT:TTTTTTTTTTT
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
T=0.00004/1 (TOMMO)
-=0.00301/3 (GoNL)
HGVS:: NC_000001.11:g.75758061_75758064del, NC_000001.11:g.75758064del, NC_000001.11:g.75758064dup, NC_000001.11:g.75758063_75758064dup, NC_000001.10:g.76223746_76223749del, NC_000001.10:g.76223749del, NC_000001.10:g.76223749dup, NC_000001.10:g.76223748_76223749dup, NG_007045.2:g.38704_38707del, NG_007045.2:g.38707del, NG_007045.2:g.38707dup, NG_007045.2:g.38706_38707dup

Select item 149117903811.

rs1491179038 has merged into rs33952162 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:75735330 (GRCh38)
1:76201015 (GRCh37)
Canonical SPDI:: NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75735319:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.195487/979 (1000Genomes)
HGVS:: NC_000001.11:g.75735330_75735339del, NC_000001.11:g.75735331_75735339del, NC_000001.11:g.75735333_75735339del, NC_000001.11:g.75735334_75735339del, NC_000001.11:g.75735335_75735339del, NC_000001.11:g.75735336_75735339del, NC_000001.11:g.75735337_75735339del, NC_000001.11:g.75735338_75735339del, NC_000001.11:g.75735339del, NC_000001.11:g.75735339dup, NC_000001.11:g.75735338_75735339dup, NC_000001.11:g.75735337_75735339dup, NC_000001.11:g.75735336_75735339dup, NC_000001.11:g.75735335_75735339dup, NC_000001.11:g.75735334_75735339dup, NC_000001.10:g.76201015_76201024del, NC_000001.10:g.76201016_76201024del, NC_000001.10:g.76201018_76201024del, NC_000001.10:g.76201019_76201024del, NC_000001.10:g.76201020_76201024del, NC_000001.10:g.76201021_76201024del, NC_000001.10:g.76201022_76201024del, NC_000001.10:g.76201023_76201024del, NC_000001.10:g.76201024del, NC_000001.10:g.76201024dup, NC_000001.10:g.76201023_76201024dup, NC_000001.10:g.76201022_76201024dup, NC_000001.10:g.76201021_76201024dup, NC_000001.10:g.76201020_76201024dup, NC_000001.10:g.76201019_76201024dup, NG_007045.2:g.15973_15982del, NG_007045.2:g.15974_15982del, NG_007045.2:g.15976_15982del, NG_007045.2:g.15977_15982del, NG_007045.2:g.15978_15982del, NG_007045.2:g.15979_15982del, NG_007045.2:g.15980_15982del, NG_007045.2:g.15981_15982del, NG_007045.2:g.15982del, NG_007045.2:g.15982dup, NG_007045.2:g.15981_15982dup, NG_007045.2:g.15980_15982dup, NG_007045.2:g.15979_15982dup, NG_007045.2:g.15978_15982dup, NG_007045.2:g.15977_15982dup

Select item 149116823512.

rs1491168235 [Homo sapiens]

Variant type:: INS
Alleles:: ->ATAA,ATATAA,ATATATAA,ATATATATATATAA,ATATATATATATATATATATGA,ATATATATATATATATATGA,ATATATATATATATATGA,ATATATATATATATGA,ATATATATATATGA,ATATATATATGA,ATATATATGA,ATATATATGG,ATATATGA,ATATGA,ATGA [Show Flanks]
Chromosome:: 1:75737327 (GRCh38)
1:76203013 (GRCh37)
Canonical SPDI:: NC_000001.11:75737327::ATAA,NC_000001.11:75737327::ATATAA,NC_000001.11:75737327::ATATATAA,NC_000001.11:75737327::ATATATATATATAA,NC_000001.11:75737327::ATATATATATATATATATATGA,NC_000001.11:75737327::ATATATATATATATATATGA,NC_000001.11:75737327::ATATATATATATATATGA,NC_000001.11:75737327::ATATATATATATATGA,NC_000001.11:75737327::ATATATATATATGA,NC_000001.11:75737327::ATATATATATGA,NC_000001.11:75737327::ATATATATGA,NC_000001.11:75737327::ATATATATGG,NC_000001.11:75737327::ATATATGA,NC_000001.11:75737327::ATATGA,NC_000001.11:75737327::ATGA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATGA=0.00008/1 (ALFA)
HGVS:: NC_000001.11:g.75737327_75737328insATAA, NC_000001.11:g.75737327_75737328insATATAA, NC_000001.11:g.75737327_75737328insATATATAA, NC_000001.11:g.75737327_75737328insATATATATATATAA, NC_000001.11:g.75737327_75737328insATATATATATATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATATGA, NC_000001.11:g.75737327_75737328insATATATATGA, NC_000001.11:g.75737327_75737328insATATATATGG, NC_000001.11:g.75737327_75737328insATATATGA, NC_000001.11:g.75737327_75737328insATATGA, NC_000001.11:g.75737327_75737328insATGA, NC_000001.10:g.76203012_76203013insATAA, NC_000001.10:g.76203012_76203013insATATAA, NC_000001.10:g.76203012_76203013insATATATAA, NC_000001.10:g.76203012_76203013insATATATATATATAA, NC_000001.10:g.76203012_76203013insATATATATATATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATATGA, NC_000001.10:g.76203012_76203013insATATATATGA, NC_000001.10:g.76203012_76203013insATATATATGG, NC_000001.10:g.76203012_76203013insATATATGA, NC_000001.10:g.76203012_76203013insATATGA, NC_000001.10:g.76203012_76203013insATGA, NG_007045.2:g.17970_17971insATAA, NG_007045.2:g.17970_17971insATATAA, NG_007045.2:g.17970_17971insATATATAA, NG_007045.2:g.17970_17971insATATATATATATAA, NG_007045.2:g.17970_17971insATATATATATATATATATATGA, NG_007045.2:g.17970_17971insATATATATATATATATATGA, NG_007045.2:g.17970_17971insATATATATATATATATGA, NG_007045.2:g.17970_17971insATATATATATATATGA, NG_007045.2:g.17970_17971insATATATATATATGA, NG_007045.2:g.17970_17971insATATATATATGA, NG_007045.2:g.17970_17971insATATATATGA, NG_007045.2:g.17970_17971insATATATATGG, NG_007045.2:g.17970_17971insATATATGA, NG_007045.2:g.17970_17971insATATGA, NG_007045.2:g.17970_17971insATGA

Select item 149114434613.

rs1491144346 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:75731278 (GRCh38)
1:76196963 (GRCh37)
Canonical SPDI:: NC_000001.11:75731277:CA:
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00169/20 (ALFA)
-=0.00033/9 (TOMMO)
HGVS:: NC_000001.11:g.75731278_75731279del, NC_000001.10:g.76196963_76196964del, NG_007045.2:g.11921_11922del

Select item 149110983314.

rs1491109833 [Homo sapiens]

Variant type:: DELINS
Alleles:: AC>- [Show Flanks]
Chromosome:: 1:75742919 (GRCh38)
1:76208604 (GRCh37)
Canonical SPDI:: NC_000001.11:75742917:CAC:C
Gene:: ACADM (Varview), DLSTP1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.255928/1144 (ALFA)
-=0.031283/524 (TOMMO)
-=0.178638/1144 (1000Genomes)
-=0.236765/33176 (GnomAD)
-=0.281667/169 (NorthernSweden)
HGVS:: NC_000001.11:g.75742919_75742920del, NC_000001.10:g.76208604_76208605del, NG_007045.2:g.23562_23563del, NR_130749.1:n.2095_2096del

Select item 149110725115.

rs1491107251 has merged into rs56885972 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 1:75731288 (GRCh38)
1:76196973 (GRCh37)
Canonical SPDI:: NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000001.11:75731278:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.016/9 (NorthernSweden)
HGVS:: NC_000001.11:g.75731288_75731305del, NC_000001.11:g.75731289_75731305del, NC_000001.11:g.75731290_75731305del, NC_000001.11:g.75731291_75731305del, NC_000001.11:g.75731292_75731305del, NC_000001.11:g.75731293_75731305del, NC_000001.11:g.75731294_75731305del, NC_000001.11:g.75731295_75731305del, NC_000001.11:g.75731296_75731305del, NC_000001.11:g.75731297_75731305del, NC_000001.11:g.75731298_75731305del, NC_000001.11:g.75731299_75731305del, NC_000001.11:g.75731300_75731305del, NC_000001.11:g.75731301_75731305del, NC_000001.11:g.75731302_75731305del, NC_000001.11:g.75731303_75731305del, NC_000001.11:g.75731304_75731305del, NC_000001.11:g.75731305del, NC_000001.11:g.75731305dup, NC_000001.11:g.75731304_75731305dup, NC_000001.11:g.75731303_75731305dup, NC_000001.11:g.75731302_75731305dup, NC_000001.11:g.75731301_75731305dup, NC_000001.11:g.75731298_75731305dup, NC_000001.11:g.75731297_75731305dup, NC_000001.10:g.76196973_76196990del, NC_000001.10:g.76196974_76196990del, NC_000001.10:g.76196975_76196990del, NC_000001.10:g.76196976_76196990del, NC_000001.10:g.76196977_76196990del, NC_000001.10:g.76196978_76196990del, NC_000001.10:g.76196979_76196990del, NC_000001.10:g.76196980_76196990del, NC_000001.10:g.76196981_76196990del, NC_000001.10:g.76196982_76196990del, NC_000001.10:g.76196983_76196990del, NC_000001.10:g.76196984_76196990del, NC_000001.10:g.76196985_76196990del, NC_000001.10:g.76196986_76196990del, NC_000001.10:g.76196987_76196990del, NC_000001.10:g.76196988_76196990del, NC_000001.10:g.76196989_76196990del, NC_000001.10:g.76196990del, NC_000001.10:g.76196990dup, NC_000001.10:g.76196989_76196990dup, NC_000001.10:g.76196988_76196990dup, NC_000001.10:g.76196987_76196990dup, NC_000001.10:g.76196986_76196990dup, NC_000001.10:g.76196983_76196990dup, NC_000001.10:g.76196982_76196990dup, NG_007045.2:g.11931_11948del, NG_007045.2:g.11932_11948del, NG_007045.2:g.11933_11948del, NG_007045.2:g.11934_11948del, NG_007045.2:g.11935_11948del, NG_007045.2:g.11936_11948del, NG_007045.2:g.11937_11948del, NG_007045.2:g.11938_11948del, NG_007045.2:g.11939_11948del, NG_007045.2:g.11940_11948del, NG_007045.2:g.11941_11948del, NG_007045.2:g.11942_11948del, NG_007045.2:g.11943_11948del, NG_007045.2:g.11944_11948del, NG_007045.2:g.11945_11948del, NG_007045.2:g.11946_11948del, NG_007045.2:g.11947_11948del, NG_007045.2:g.11948del, NG_007045.2:g.11948dup, NG_007045.2:g.11947_11948dup, NG_007045.2:g.11946_11948dup, NG_007045.2:g.11945_11948dup, NG_007045.2:g.11944_11948dup, NG_007045.2:g.11941_11948dup, NG_007045.2:g.11940_11948dup

Select item 149110103416.

rs1491101034 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:75726800 (GRCh38)
1:76192485 (GRCh37)
Canonical SPDI:: NC_000001.11:75726799:CT:
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.75726800_75726801del, NC_000001.10:g.76192485_76192486del, NG_007045.2:g.7443_7444del

Select item 149109670617.

rs1491096706 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 1:75773441 (GRCh38)
1:76239127 (GRCh37)
Canonical SPDI:: NC_000001.11:75773441::G
Validated:: by frequency,by alfa
MAF:: G=0.00008/1 (ALFA)
HGVS:: NC_000001.11:g.75773441_75773442insG, NC_000001.10:g.76239126_76239127insG, NG_007045.2:g.54084_54085insG

Select item 149108922718.

rs1491089227 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 1:75723407 (GRCh38)
1:76189092 (GRCh37)
Canonical SPDI:: NC_000001.11:75723404:CACA:CA
Gene:: ACADM (Varview), SLC44A5 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACA=0./0 (ALFA)
-=0.00004/0 (TOMMO)
HGVS:: NC_000001.11:g.75723405CA[1], NC_000001.10:g.76189090CA[1], NG_007045.2:g.4048CA[1]

Select item 149107057819.

rs1491070578 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:75773463 (GRCh38)
1:76239148 (GRCh37)
Canonical SPDI:: NC_000001.11:75773461:AGA:A
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
HGVS:: NC_000001.11:g.75773463_75773464del, NC_000001.10:g.76239148_76239149del, NG_007045.2:g.54106_54107del

Select item 149106303920.

rs1491063039 has merged into rs3831899 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 1:75726375 (GRCh38)
1:76192060 (GRCh37)
Canonical SPDI:: NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000001.11:75726366:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: ACADM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.0937/469 (1000Genomes)
HGVS:: NC_000001.11:g.75726375_75726380del, NC_000001.11:g.75726376_75726380del, NC_000001.11:g.75726379_75726380del, NC_000001.11:g.75726380del, NC_000001.11:g.75726380dup, NC_000001.11:g.75726379_75726380dup, NC_000001.11:g.75726378_75726380dup, NC_000001.11:g.75726377_75726380dup, NC_000001.11:g.75726376_75726380dup, NC_000001.10:g.76192060_76192065del, NC_000001.10:g.76192061_76192065del, NC_000001.10:g.76192064_76192065del, NC_000001.10:g.76192065del, NC_000001.10:g.76192065dup, NC_000001.10:g.76192064_76192065dup, NC_000001.10:g.76192063_76192065dup, NC_000001.10:g.76192062_76192065dup, NC_000001.10:g.76192061_76192065dup, NG_007045.2:g.7018_7023del, NG_007045.2:g.7019_7023del, NG_007045.2:g.7022_7023del, NG_007045.2:g.7023del, NG_007045.2:g.7023dup, NG_007045.2:g.7022_7023dup, NG_007045.2:g.7021_7023dup, NG_007045.2:g.7020_7023dup, NG_007045.2:g.7019_7023dup

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