SNP Links for Gene (Select 84619) - SNP

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Select item 14915712831.

rs1491571283 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 20:63732099 (GRCh38)
20:62363451 (GRCh37)
Canonical SPDI:: NC_000020.11:63732095:TGTGT:TGT
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.63732097GT[1], NC_000020.10:g.62363449GT[1]

Select item 14915708262.

rs1491570826 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 20:63724364 (GRCh38)
20:62355717 (GRCh37)
Canonical SPDI:: NC_000020.11:63724364::G
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.0003/3 (GnomAD)
HGVS:: NC_000020.11:g.63724364_63724365insG, NC_000020.10:g.62355716_62355717insG

Select item 14915694363.

rs1491569436 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 20:63730017 (GRCh38)
20:62361369 (GRCh37)
Canonical SPDI:: NC_000020.11:63730016:TG:
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: -=0.00011/2 (GnomAD)
HGVS:: NC_000020.11:g.63730017_63730018del, NC_000020.10:g.62361369_62361370del

Select item 14915670934.

rs1491567093 [Homo sapiens]

Variant type:: INS
Alleles:: ->TT [Show Flanks]
Chromosome:: 20:63732681 (GRCh38)
20:62364034 (GRCh37)
Canonical SPDI:: NC_000020.11:63732681::TT
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
TT=0.00011/6 (GnomAD)
HGVS:: NC_000020.11:g.63732681_63732682insTT, NC_000020.10:g.62364033_62364034insTT

Select item 14915649365.

rs1491564936 has merged into rs58067228 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACACA>-,CACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA [Show Flanks]
Chromosome:: 20:63730043 (GRCh38)
20:62361395 (GRCh37)
Canonical SPDI:: NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA,NC_000020.11:63730020:CACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACA
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACACACACACACACACACACACA=0./0 (ALFA)
HGVS:: NC_000020.11:g.63730021CA[11], NC_000020.11:g.63730021CA[13], NC_000020.11:g.63730021CA[15], NC_000020.11:g.63730021CA[16], NC_000020.11:g.63730021CA[17], NC_000020.11:g.63730021CA[18], NC_000020.11:g.63730021CA[19], NC_000020.11:g.63730021CA[20], NC_000020.11:g.63730021CA[21], NC_000020.11:g.63730021CA[22], NC_000020.11:g.63730021CA[23], NC_000020.11:g.63730021CA[24], NC_000020.10:g.62361373CA[11], NC_000020.10:g.62361373CA[13], NC_000020.10:g.62361373CA[15], NC_000020.10:g.62361373CA[16], NC_000020.10:g.62361373CA[17], NC_000020.10:g.62361373CA[18], NC_000020.10:g.62361373CA[19], NC_000020.10:g.62361373CA[20], NC_000020.10:g.62361373CA[21], NC_000020.10:g.62361373CA[22], NC_000020.10:g.62361373CA[23], NC_000020.10:g.62361373CA[24]

Select item 14915479256.

rs1491547925 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TG [Show Flanks]
Chromosome:: 20:63732427 (GRCh38)
20:62363780 (GRCh37)
Canonical SPDI:: NC_000020.11:63732427:TGTGTG:TGTGTGTG
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGTGTGTG=0./0 (ALFA)
TG=0.00004/1 (GnomAD)
HGVS:: NC_000020.11:g.63732428TG[4], NC_000020.10:g.62363780TG[4]

Select item 14915035857.

rs1491503585 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 20:63727690 (GRCh38)
20:62359043 (GRCh37)
Canonical SPDI:: NC_000020.11:63727690:GG:GGG
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GGG=0.000084/1 (ALFA)
G=0.000043/6 (GnomAD)
HGVS:: NC_000020.11:g.63727692dup, NC_000020.10:g.62359044dup

Select item 14914918818.

rs1491491881 [Homo sapiens]

Variant type:: INS
Alleles:: ->CC,GGTGTGTGCGCGCATGTGTGTGGGTGAGGGCC [Show Flanks]
Chromosome:: 20:63732368 (GRCh38)
20:62363721 (GRCh37)
Canonical SPDI:: NC_000020.11:63732368::CC,NC_000020.11:63732368::GGTGTGTGCGCGCATGTGTGTGGGTGAGGGCC
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0.00531/14 (ALFA)
CC=0.00109/2 (Korea1K)
CC=0.00133/22 (TOMMO)
HGVS:: NC_000020.11:g.63732368_63732369insCC, NC_000020.11:g.63732368_63732369insGGTGTGTGCGCGCATGTGTGTGGGTGAGGGCC, NC_000020.10:g.62363720_62363721insCC, NC_000020.10:g.62363720_62363721insGGTGTGTGCGCGCATGTGTGTGGGTGAGGGCC

Select item 14914780799.

rs1491478079 [Homo sapiens]

Variant type:: DELINS
Alleles:: GC>- [Show Flanks]
Chromosome:: 20:63730020 (GRCh38)
20:62361372 (GRCh37)
Canonical SPDI:: NC_000020.11:63730017:GCGC:GC
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GCGC=0.00017/2 (ALFA)
-=0.00792/39 (GnomAD)
HGVS:: NC_000020.11:g.63730018GC[1], NC_000020.10:g.62361370GC[1]

Select item 149145887510.

rs1491458875 [Homo sapiens]

Variant type:: DEL
Alleles:: AG>- [Show Flanks]
Chromosome:: 20:63727690 (GRCh38)
20:62359042 (GRCh37)
Canonical SPDI:: NC_000020.11:63727689:AG:
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000020.11:g.63727690_63727691del, NC_000020.10:g.62359042_62359043del

Select item 149144832411.

rs1491448324 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 20:63732681 (GRCh38)
20:62364033 (GRCh37)
Canonical SPDI:: NC_000020.11:63732680:CA:
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000020.11:g.63732681_63732682del, NC_000020.10:g.62364033_62364034del

Select item 149142694612.

rs1491426946 has merged into rs11472431 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGT>-,GT,GTGTGT,GTGTGTGT [Show Flanks]
Chromosome:: 20:63732656 (GRCh38)
20:62364008 (GRCh37)
Canonical SPDI:: NC_000020.11:63732650:TGTGTGTGT:TGTGT,NC_000020.11:63732650:TGTGTGTGT:TGTGTGT,NC_000020.11:63732650:TGTGTGTGT:TGTGTGTGTGT,NC_000020.11:63732650:TGTGTGTGT:TGTGTGTGTGTGT
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGT=0./0 (ALFA)
TG=0.127/186 (1000Genomes)
HGVS:: NC_000020.11:g.63732652GT[2], NC_000020.11:g.63732652GT[3], NC_000020.11:g.63732652GT[5], NC_000020.11:g.63732652GT[6], NC_000020.10:g.62364004GT[2], NC_000020.10:g.62364004GT[3], NC_000020.10:g.62364004GT[5], NC_000020.10:g.62364004GT[6]

Select item 149141656413.

rs1491416564 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 20:63722016 (GRCh38)
20:62353368 (GRCh37)
Canonical SPDI:: NC_000020.11:63722015:GA:
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00001/1 (GnomAD)
HGVS:: NC_000020.11:g.63722016_63722017del, NC_000020.10:g.62353368_62353369del

Select item 149140074414.

rs1491400744 has merged into rs113843559 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTGTGT>-,GT,GTGT,GTGTGTGT [Show Flanks]
Chromosome:: 20:63733042 (GRCh38)
20:62364394 (GRCh37)
Canonical SPDI:: NC_000020.11:63733036:TGTGTGTGTGT:TGTGT,NC_000020.11:63733036:TGTGTGTGTGT:TGTGTGT,NC_000020.11:63733036:TGTGTGTGTGT:TGTGTGTGT,NC_000020.11:63733036:TGTGTGTGTGT:TGTGTGTGTGTGT
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTGTGTGTGTGT=0./0 (ALFA)
-=0.000034/9 (TOPMED)
-=0.01473/73 (1000Genomes)
-=0.033333/20 (NorthernSweden)
HGVS:: NC_000020.11:g.63733038GT[2], NC_000020.11:g.63733038GT[3], NC_000020.11:g.63733038GT[4], NC_000020.11:g.63733038GT[6], NC_000020.10:g.62364390GT[2], NC_000020.10:g.62364390GT[3], NC_000020.10:g.62364390GT[4], NC_000020.10:g.62364390GT[6]

Select item 149138963415.

rs1491389634 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTC [Show Flanks]
Chromosome:: 20:63730923 (GRCh38)
20:62362276 (GRCh37)
Canonical SPDI:: NC_000020.11:63730923:CTC:CTCCCTC
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCCCTC=0./0 (ALFA)
CTCC=0.00111/18 (TOMMO)
HGVS:: NC_000020.11:g.63730926_63730927insCCTC, NC_000020.10:g.62362278_62362279insCCTC

Select item 149138472516.

rs1491384725 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 20:63732844 (GRCh38)
20:62364196 (GRCh37)
Canonical SPDI:: NC_000020.11:63732843:AT:
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000015/4 (TOPMED)
HGVS:: NC_000020.11:g.63732844_63732845del, NC_000020.10:g.62364196_62364197del

Select item 149134517117.

rs1491345171 has merged into rs1295612883 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGTGTGTG>-,TG,TGTG,TGTGTG [Show Flanks]
Chromosome:: 20:63732411 (GRCh38)
20:62363763 (GRCh37)
Canonical SPDI:: NC_000020.11:63732409:GTGTGTGTG:G,NC_000020.11:63732409:GTGTGTGTG:GTG,NC_000020.11:63732409:GTGTGTGTG:GTGTG,NC_000020.11:63732409:GTGTGTGTG:GTGTGTG
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGTG=0./0 (ALFA)
-=0.00299/50 (TOMMO)
HGVS:: NC_000020.11:g.63732411_63732418del, NC_000020.11:g.63732411TG[1], NC_000020.11:g.63732411TG[2], NC_000020.11:g.63732411TG[3], NC_000020.10:g.62363763_62363770del, NC_000020.10:g.62363763TG[1], NC_000020.10:g.62363763TG[2], NC_000020.10:g.62363763TG[3]

Select item 149130852718.

rs1491308527 has merged into rs11320808 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA [Show Flanks]
Chromosome:: 20:63722031 (GRCh38)
20:62353383 (GRCh37)
Canonical SPDI:: NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000020.11:63722016:AAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.0298/115 (ALSPAC)
HGVS:: NC_000020.11:g.63722031_63722034del, NC_000020.11:g.63722032_63722034del, NC_000020.11:g.63722033_63722034del, NC_000020.11:g.63722034del, NC_000020.11:g.63722034dup, NC_000020.11:g.63722033_63722034dup, NC_000020.10:g.62353383_62353386del, NC_000020.10:g.62353384_62353386del, NC_000020.10:g.62353385_62353386del, NC_000020.10:g.62353386del, NC_000020.10:g.62353386dup, NC_000020.10:g.62353385_62353386dup

Select item 149128020019.

rs1491280200 has merged into rs33915732 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCTCTCTCTCTCTCTCTCTCTCTCTCT>-,CT,CTCT,CTCTCT,CTCTCTCT,CTCTCTCTCT,CTCTCTCTCTCT,CTCTCTCTCTCTCT,CTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,CTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT [Show Flanks]
Chromosome:: 20:63730942 (GRCh38)
20:62362294 (GRCh37)
Canonical SPDI:: NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT,NC_000020.11:63730922:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT:TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCT
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCTCTCTCTCTCT=0./0 (ALFA)
TCTCTC=0.5/20 (GENOME_DK)
HGVS:: NC_000020.11:g.63730924CT[9], NC_000020.11:g.63730924CT[10], NC_000020.11:g.63730924CT[11], NC_000020.11:g.63730924CT[12], NC_000020.11:g.63730924CT[13], NC_000020.11:g.63730924CT[14], NC_000020.11:g.63730924CT[15], NC_000020.11:g.63730924CT[16], NC_000020.11:g.63730924CT[17], NC_000020.11:g.63730924CT[18], NC_000020.11:g.63730924CT[19], NC_000020.11:g.63730924CT[20], NC_000020.11:g.63730924CT[21], NC_000020.11:g.63730924CT[22], NC_000020.11:g.63730924CT[23], NC_000020.11:g.63730924CT[25], NC_000020.11:g.63730924CT[26], NC_000020.11:g.63730924CT[27], NC_000020.11:g.63730924CT[28], NC_000020.11:g.63730924CT[29], NC_000020.11:g.63730924CT[30], NC_000020.11:g.63730924CT[31], NC_000020.11:g.63730924CT[32], NC_000020.11:g.63730924CT[33], NC_000020.11:g.63730924CT[34], NC_000020.10:g.62362276CT[9], NC_000020.10:g.62362276CT[10], NC_000020.10:g.62362276CT[11], NC_000020.10:g.62362276CT[12], NC_000020.10:g.62362276CT[13], NC_000020.10:g.62362276CT[14], NC_000020.10:g.62362276CT[15], NC_000020.10:g.62362276CT[16], NC_000020.10:g.62362276CT[17], NC_000020.10:g.62362276CT[18], NC_000020.10:g.62362276CT[19], NC_000020.10:g.62362276CT[20], NC_000020.10:g.62362276CT[21], NC_000020.10:g.62362276CT[22], NC_000020.10:g.62362276CT[23], NC_000020.10:g.62362276CT[25], NC_000020.10:g.62362276CT[26], NC_000020.10:g.62362276CT[27], NC_000020.10:g.62362276CT[28], NC_000020.10:g.62362276CT[29], NC_000020.10:g.62362276CT[30], NC_000020.10:g.62362276CT[31], NC_000020.10:g.62362276CT[32], NC_000020.10:g.62362276CT[33], NC_000020.10:g.62362276CT[34]

Select item 149127576620.

rs1491275766 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ACGC [Show Flanks]
Chromosome:: 20:63730017 (GRCh38)
20:62361370 (GRCh37)
Canonical SPDI:: NC_000020.11:63730017:GC:GCACGC
Gene:: ZGPAT (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GCACGC=0./0 (ALFA)
GCAC=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.63730019_63730020insACGC, NC_000020.10:g.62361371_62361372insACGC

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