SNP Links for Gene (Select 3820) - SNP

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Select item 14915746321.

rs1491574632 has merged into rs1414131200 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AAAAA [Show Flanks]
Chromosome:: 12:9606665 (GRCh38)
12:9759261 (GRCh37)
Canonical SPDI:: NC_000012.12:9606663:AAAA:A,NC_000012.12:9606663:AAAA:AA,NC_000012.12:9606663:AAAA:AAAAAA
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606665_9606667del, NC_000012.12:g.9606666_9606667del, NC_000012.12:g.9606666_9606667dup, NC_000012.11:g.9759261_9759263del, NC_000012.11:g.9759262_9759263del, NC_000012.11:g.9759262_9759263dup

Select item 14915742262.

rs1491574226 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 12:9607334 (GRCh38)
12:9759930 (GRCh37)
Canonical SPDI:: NC_000012.12:9607333:TC:
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: -=0.00017/4 (GnomAD)
HGVS:: NC_000012.12:g.9607334_9607335del, NC_000012.11:g.9759930_9759931del

Select item 14915578443.

rs1491557844 has merged into rs1352001438 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T [Show Flanks]
Chromosome:: 12:9607318 (GRCh38)
12:9759914 (GRCh37)
Canonical SPDI:: NC_000012.12:9607316:TTTT:T,NC_000012.12:9607316:TTTT:TT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
HGVS:: NC_000012.12:g.9607318_9607320del, NC_000012.12:g.9607319_9607320del, NC_000012.11:g.9759914_9759916del, NC_000012.11:g.9759915_9759916del

Select item 14915228264.

rs1491522826 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 12:9606691 (GRCh38)
12:9759287 (GRCh37)
Canonical SPDI:: NC_000012.12:9606690:GT:
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000017/1 (GnomAD)
HGVS:: NC_000012.12:g.9606691_9606692del, NC_000012.11:g.9759287_9759288del

Select item 14915216625.

rs1491521662 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>-,CTCT,CTCTCT [Show Flanks]
Chromosome:: 12:9607364 (GRCh38)
12:9759960 (GRCh37)
Canonical SPDI:: NC_000012.12:9607362:TCT:T,NC_000012.12:9607362:TCT:TCTCT,NC_000012.12:9607362:TCT:TCTCTCT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000012.12:g.9607364_9607365del, NC_000012.12:g.9607364_9607365dup, NC_000012.12:g.9607364CT[3], NC_000012.11:g.9759960_9759961del, NC_000012.11:g.9759960_9759961dup, NC_000012.11:g.9759960CT[3]

Select item 14915105816.

rs1491510581 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTT [Show Flanks]
Chromosome:: 12:9607363 (GRCh38)
12:9759960 (GRCh37)
Canonical SPDI:: NC_000012.12:9607363:CTT:CTTCCTT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: CTTCCTT=0./0 (ALFA)
CTTC=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.9607366_9607367insCCTT, NC_000012.11:g.9759962_9759963insCCTT

Select item 14915050107.

rs1491505010 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TCT,TT,TTCCTTCCTTCCTTT,TTCCTTCCTTCCTTTCTTT,TTCCTTCCTTCCTTTCTTTCTTTCTTT,TTCCTTCCTTCCTTTCTTTCTTTCTTTCTTT,TTCCTTCCTTT,TTCCTTCCTTTCTTT,TTCCTTCCTTTCTTTCTTT,TTCCTTCCTTTCTTTCTTTCTTT,TTCCTTCCTTTCTTTCTTTCTTTCTTT,TTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT,TTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,TTCCTTCGTTT,TTCCTTCGTTTCTTT,TTCCTTCGTTTCTTTCTTT,TTCCTTCGTTTCTTTCTTTCTTT,TTCCTTT,TTCCTTTCTTTCTTTCTTT,TTT,TTTCTCTTTCTTTTCTTTCTTTCTTT,TTTCTCTTTCTTTTCTTTCTTTCTTTCTTT,TTTCTTCCTTCCTTCCTTT,TTTCTTCCTTCCTTCCTTTCTTT,TTTCTTCCTTCCTTCCTTTCTTTCTTT,TTTCTTCCTTCCTTT,TTTCTTCCTTCCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTT,TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,TTTCTTCCTTT,TTTCTTCCTTTCTTTCTTT,TTTCTTT,TTTCTTTCTTCCTTTCTTT,TTTCTTTCTTT,TTTCTTTCTTTCTCTCTTT,TTTCTTTCTTTCTTT,TTTCTTTCTTTCTTTCTTT,TTTCTTTCTTTCTTTCTTTCTTT,TTTCTTTCTTTCTTTCTTTCTTTCTTT,TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,TTTT [Show Flanks]
Chromosome:: 12:9607335 (GRCh38)
12:9759932 (GRCh37)
Canonical SPDI:: NC_000012.12:9607335::T,NC_000012.12:9607335::TCT,NC_000012.12:9607335::TT,NC_000012.12:9607335::TTCCTTCCTTCCTTT,NC_000012.12:9607335::TTCCTTCCTTCCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTCCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTCCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCGTTT,NC_000012.12:9607335::TTCCTTCGTTTCTTT,NC_000012.12:9607335::TTCCTTCGTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTCGTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTCCTTT,NC_000012.12:9607335::TTCCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTT,NC_000012.12:9607335::TTTCTCTTTCTTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTCTTTCTTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTCCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTCCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTCCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTCCTTT,NC_000012.12:9607335::TTTCTTCCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTT,NC_000012.12:9607335::TTTCTTTCTTCCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTCTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT,NC_000012.12:9607335::TTTT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0./0 (ALFA)
HGVS:: NC_000012.12:g.9607335_9607336insT, NC_000012.12:g.9607335_9607336insTCT, NC_000012.12:g.9607335_9607336insTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTCCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTCCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCGTTT, NC_000012.12:g.9607335_9607336insTTCCTTCGTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCGTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTCGTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTCCTTT, NC_000012.12:g.9607335_9607336insTTCCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTT, NC_000012.12:g.9607335_9607336insTTTCTCTTTCTTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTCTTTCTTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTCCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTCCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTCCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTT, NC_000012.12:g.9607335_9607336insTTTCTTCCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTCCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTCTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.12:g.9607335_9607336insTTTT, NC_000012.11:g.9759931_9759932insT, NC_000012.11:g.9759931_9759932insTCT, NC_000012.11:g.9759931_9759932insTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTCCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTCCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCGTTT, NC_000012.11:g.9759931_9759932insTTCCTTCGTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCGTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTCGTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTCCTTT, NC_000012.11:g.9759931_9759932insTTCCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTT, NC_000012.11:g.9759931_9759932insTTTCTCTTTCTTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTCTTTCTTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTCCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTCCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTCCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTCCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTT, NC_000012.11:g.9759931_9759932insTTTCTTCCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTCCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTCTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTT, NC_000012.11:g.9759931_9759932insTTTT

Select item 14914261878.

rs1491426187 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ACA [Show Flanks]
Chromosome:: 12:9603599 (GRCh38)
12:9756196 (GRCh37)
Canonical SPDI:: NC_000012.12:9603599::A,NC_000012.12:9603599::ACA
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACA=0./0 (ALFA)
A=0.00214/2 (GnomAD)
HGVS:: NC_000012.12:g.9603599_9603600insA, NC_000012.12:g.9603599_9603600insACA, NC_000012.11:g.9756195_9756196insA, NC_000012.11:g.9756195_9756196insACA

Select item 14913928209.

rs1491392820 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 12:9607275 (GRCh38)
12:9759872 (GRCh37)
Canonical SPDI:: NC_000012.12:9607275:C:CC
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
C=0.00069/1 (Korea1K)
C=0.00071/55 (GnomAD)
HGVS:: NC_000012.12:g.9607276dup, NC_000012.11:g.9759872dup

Select item 149137830910.

rs1491378309 has merged into rs55659351 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAAA,AAAAAAAAA [Show Flanks]
Chromosome:: 12:9599990 (GRCh38)
12:9752586 (GRCh37)
Canonical SPDI:: NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000012.12:9599980:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
AAA=0.2177/633 (1000Genomes)
HGVS:: NC_000012.12:g.9599990_9599996del, NC_000012.12:g.9599991_9599996del, NC_000012.12:g.9599992_9599996del, NC_000012.12:g.9599993_9599996del, NC_000012.12:g.9599994_9599996del, NC_000012.12:g.9599995_9599996del, NC_000012.12:g.9599996del, NC_000012.12:g.9599996dup, NC_000012.12:g.9599995_9599996dup, NC_000012.11:g.9752586_9752592del, NC_000012.11:g.9752587_9752592del, NC_000012.11:g.9752588_9752592del, NC_000012.11:g.9752589_9752592del, NC_000012.11:g.9752590_9752592del, NC_000012.11:g.9752591_9752592del, NC_000012.11:g.9752592del, NC_000012.11:g.9752592dup, NC_000012.11:g.9752591_9752592dup

Select item 149126995111.

rs1491269951 [Homo sapiens]

Variant type:: DEL
Alleles:: GT>- [Show Flanks]
Chromosome:: 12:9606734 (GRCh38)
12:9759330 (GRCh37)
Canonical SPDI:: NC_000012.12:9606733:GT:
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606734_9606735del, NC_000012.11:g.9759330_9759331del

Select item 149121939512.

rs1491219395 has merged into rs1555097706 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCTCT>-,CT,CTCT,CTCTCTCT [Show Flanks]
Chromosome:: 12:9607278 (GRCh38)
12:9759874 (GRCh37)
Canonical SPDI:: NC_000012.12:9607274:TCTCTCTCT:TCT,NC_000012.12:9607274:TCTCTCTCT:TCTCT,NC_000012.12:9607274:TCTCTCTCT:TCTCTCT,NC_000012.12:9607274:TCTCTCTCT:TCTCTCTCTCT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCT=0./0 (ALFA)
-=0.00004/3 (GnomAD)
-=0.00016/1 (1000Genomes)
HGVS:: NC_000012.12:g.9607276CT[1], NC_000012.12:g.9607276CT[2], NC_000012.12:g.9607276CT[3], NC_000012.12:g.9607276CT[5], NC_000012.11:g.9759872CT[1], NC_000012.11:g.9759872CT[2], NC_000012.11:g.9759872CT[3], NC_000012.11:g.9759872CT[5]

Select item 149121771813.

rs1491217718 has merged into rs1234515362 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATATATATAT>-,AT,ATAT,ATATAT,ATATATAT,ATATATATATAT,ATATATATATATAT,ATATATATATATATAT,ATATATATATATATATAT,ATATATATATATATATATAT,ATATATATATATATATATATAT [Show Flanks]
Chromosome:: 12:9606752 (GRCh38)
12:9759348 (GRCh37)
Canonical SPDI:: NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATAT,NC_000012.12:9606734:TATATATATATATATATATATATATAT:TATATATATATATATATATATATATATATATATATATAT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATATATAT=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606736AT[8], NC_000012.12:g.9606736AT[9], NC_000012.12:g.9606736AT[10], NC_000012.12:g.9606736AT[11], NC_000012.12:g.9606736AT[12], NC_000012.12:g.9606736AT[14], NC_000012.12:g.9606736AT[15], NC_000012.12:g.9606736AT[16], NC_000012.12:g.9606736AT[17], NC_000012.12:g.9606736AT[18], NC_000012.12:g.9606736AT[19], NC_000012.11:g.9759332AT[8], NC_000012.11:g.9759332AT[9], NC_000012.11:g.9759332AT[10], NC_000012.11:g.9759332AT[11], NC_000012.11:g.9759332AT[12], NC_000012.11:g.9759332AT[14], NC_000012.11:g.9759332AT[15], NC_000012.11:g.9759332AT[16], NC_000012.11:g.9759332AT[17], NC_000012.11:g.9759332AT[18], NC_000012.11:g.9759332AT[19]

Select item 149120353614.

rs1491203536 [Homo sapiens]

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

Select item 149117445115.

rs1491174451 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATG [Show Flanks]
Chromosome:: 12:9606761 (GRCh38)
12:9759358 (GRCh37)
Canonical SPDI:: NC_000012.12:9606761::A,NC_000012.12:9606761::ATA,NC_000012.12:9606761::ATATA,NC_000012.12:9606761::ATATATA,NC_000012.12:9606761::ATATATATA,NC_000012.12:9606761::ATATATATATA,NC_000012.12:9606761::ATATATATATATA,NC_000012.12:9606761::ATATATATATATATA,NC_000012.12:9606761::ATATATATATATATATA,NC_000012.12:9606761::ATG
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606761_9606762insA, NC_000012.12:g.9606761_9606762insATA, NC_000012.12:g.9606761_9606762insATATA, NC_000012.12:g.9606761_9606762insATATATA, NC_000012.12:g.9606761_9606762insATATATATA, NC_000012.12:g.9606761_9606762insATATATATATA, NC_000012.12:g.9606761_9606762insATATATATATATA, NC_000012.12:g.9606761_9606762insATATATATATATATA, NC_000012.12:g.9606761_9606762insATATATATATATATATA, NC_000012.12:g.9606761_9606762insATG, NC_000012.11:g.9759357_9759358insA, NC_000012.11:g.9759357_9759358insATA, NC_000012.11:g.9759357_9759358insATATA, NC_000012.11:g.9759357_9759358insATATATA, NC_000012.11:g.9759357_9759358insATATATATA, NC_000012.11:g.9759357_9759358insATATATATATA, NC_000012.11:g.9759357_9759358insATATATATATATA, NC_000012.11:g.9759357_9759358insATATATATATATATA, NC_000012.11:g.9759357_9759358insATATATATATATATATA, NC_000012.11:g.9759357_9759358insATG

Select item 149116589016.

rs1491165890 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 12:9607317 (GRCh38)
12:9759914 (GRCh37)
Canonical SPDI:: NC_000012.12:9607317::C
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000012.12:g.9607317_9607318insC, NC_000012.11:g.9759913_9759914insC

Select item 149112420317.

rs1491124203 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CCTTCCTGCCTGCCTGCCTT,CCTTCCTGCCTGCCTT,CCTTCCTGCCTT [Show Flanks]
Chromosome:: 12:9607334 (GRCh38)
12:9759931 (GRCh37)
Canonical SPDI:: NC_000012.12:9607334:CCTT:CCTTCCTTCCTGCCTGCCTGCCTT,NC_000012.12:9607334:CCTT:CCTTCCTTCCTGCCTGCCTT,NC_000012.12:9607334:CCTT:CCTTCCTTCCTGCCTT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
HGVS:: NC_000012.12:g.9607335_9607338CCTT[2]CCTG[3]CCTT[1], NC_000012.12:g.9607335_9607338CCTT[2]CCTG[2]CCTT[1], NC_000012.12:g.9607335_9607338CCTT[2]CCTGCCTT[1], NC_000012.11:g.9759931_9759934CCTT[2]CCTG[3]CCTT[1], NC_000012.11:g.9759931_9759934CCTT[2]CCTG[2]CCTT[1], NC_000012.11:g.9759931_9759934CCTT[2]CCTGCCTT[1]

Select item 149109488118.

rs1491094881 has merged into rs1185510083 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 12:9606768 (GRCh38)
12:9759364 (GRCh37)
Canonical SPDI:: NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000012.12:9606760:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606768_9606776del, NC_000012.12:g.9606770_9606776del, NC_000012.12:g.9606772_9606776del, NC_000012.12:g.9606773_9606776del, NC_000012.12:g.9606774_9606776del, NC_000012.12:g.9606775_9606776del, NC_000012.12:g.9606776del, NC_000012.12:g.9606776dup, NC_000012.12:g.9606775_9606776dup, NC_000012.12:g.9606774_9606776dup, NC_000012.12:g.9606773_9606776dup, NC_000012.12:g.9606772_9606776dup, NC_000012.12:g.9606771_9606776dup, NC_000012.12:g.9606770_9606776dup, NC_000012.12:g.9606769_9606776dup, NC_000012.12:g.9606768_9606776dup, NC_000012.12:g.9606767_9606776dup, NC_000012.12:g.9606766_9606776dup, NC_000012.12:g.9606765_9606776dup, NC_000012.12:g.9606764_9606776dup, NC_000012.12:g.9606763_9606776dup, NC_000012.12:g.9606762_9606776dup, NC_000012.12:g.9606761_9606776dup, NC_000012.12:g.9606776_9606777insTTTTTTTTTTTTTTTTTTT, NC_000012.11:g.9759364_9759372del, NC_000012.11:g.9759366_9759372del, NC_000012.11:g.9759368_9759372del, NC_000012.11:g.9759369_9759372del, NC_000012.11:g.9759370_9759372del, NC_000012.11:g.9759371_9759372del, NC_000012.11:g.9759372del, NC_000012.11:g.9759372dup, NC_000012.11:g.9759371_9759372dup, NC_000012.11:g.9759370_9759372dup, NC_000012.11:g.9759369_9759372dup, NC_000012.11:g.9759368_9759372dup, NC_000012.11:g.9759367_9759372dup, NC_000012.11:g.9759366_9759372dup, NC_000012.11:g.9759365_9759372dup, NC_000012.11:g.9759364_9759372dup, NC_000012.11:g.9759363_9759372dup, NC_000012.11:g.9759362_9759372dup, NC_000012.11:g.9759361_9759372dup, NC_000012.11:g.9759360_9759372dup, NC_000012.11:g.9759359_9759372dup, NC_000012.11:g.9759358_9759372dup, NC_000012.11:g.9759357_9759372dup, NC_000012.11:g.9759372_9759373insTTTTTTTTTTTTTTTTTTT

Select item 149107721119.

rs1491077211 [Homo sapiens]

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

Select item 149107095620.

rs1491070956 has merged into rs56320334 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATA>-,TA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA [Show Flanks]
Chromosome:: 12:9606704 (GRCh38)
12:9759300 (GRCh37)
Canonical SPDI:: NC_000012.12:9606691:TATATATATATATATA:TATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATATATATATATA,NC_000012.12:9606691:TATATATATATATATA:TATATATATATATATATATATATATA
Gene:: KLRB1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TATATATATATATA=0./0 (ALFA)
HGVS:: NC_000012.12:g.9606692TA[6], NC_000012.12:g.9606692TA[7], NC_000012.12:g.9606692TA[9], NC_000012.12:g.9606692TA[10], NC_000012.12:g.9606692TA[11], NC_000012.12:g.9606692TA[12], NC_000012.12:g.9606692TA[13], NC_000012.11:g.9759288TA[6], NC_000012.11:g.9759288TA[7], NC_000012.11:g.9759288TA[9], NC_000012.11:g.9759288TA[10], NC_000012.11:g.9759288TA[11], NC_000012.11:g.9759288TA[12], NC_000012.11:g.9759288TA[13]

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