SNP Links for Gene (Select 22944) - SNP

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Select item 14915874681.

rs1491587468 has merged into rs35343111 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:7765171 (GRCh38)
10:7807134 (GRCh37)
Canonical SPDI:: NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7765159:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.325/13 (GENOME_DK)
HGVS:: NC_000010.11:g.7765171_7765180del, NC_000010.11:g.7765173_7765180del, NC_000010.11:g.7765174_7765180del, NC_000010.11:g.7765175_7765180del, NC_000010.11:g.7765176_7765180del, NC_000010.11:g.7765178_7765180del, NC_000010.11:g.7765179_7765180del, NC_000010.11:g.7765180del, NC_000010.11:g.7765180dup, NC_000010.11:g.7765179_7765180dup, NC_000010.11:g.7765178_7765180dup, NC_000010.11:g.7765177_7765180dup, NC_000010.11:g.7765175_7765180dup, NC_000010.11:g.7765174_7765180dup, NC_000010.10:g.7807134_7807143del, NC_000010.10:g.7807136_7807143del, NC_000010.10:g.7807137_7807143del, NC_000010.10:g.7807138_7807143del, NC_000010.10:g.7807139_7807143del, NC_000010.10:g.7807141_7807143del, NC_000010.10:g.7807142_7807143del, NC_000010.10:g.7807143del, NC_000010.10:g.7807143dup, NC_000010.10:g.7807142_7807143dup, NC_000010.10:g.7807141_7807143dup, NC_000010.10:g.7807140_7807143dup, NC_000010.10:g.7807138_7807143dup, NC_000010.10:g.7807137_7807143dup

Select item 14915693902.

rs1491569390 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:7777053 (GRCh38)
10:7819016 (GRCh37)
Canonical SPDI:: NC_000010.11:7777052:CA:
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000010.11:g.7777053_7777054del, NC_000010.10:g.7819016_7819017del

Select item 14915215483.

rs1491521548 [Homo sapiens]

Variant type:: INS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:7785812 (GRCh38)
10:7827776 (GRCh37)
Canonical SPDI:: NC_000010.11:7785812::T
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000276/31 (GnomAD)
T=0.009879/18 (Korea1K)
HGVS:: NC_000010.11:g.7785812_7785813insT, NC_000010.10:g.7827775_7827776insT

Select item 14914155364.

rs1491415536 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 10:7754357 (GRCh38)
10:7796320 (GRCh37)
Canonical SPDI:: NC_000010.11:7754354:AGAG:AG
Gene:: KIN (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000546/1 (Korea1K)
HGVS:: NC_000010.11:g.7754355AG[1], NC_000010.10:g.7796318AG[1], NM_012311.4:c.*1722CT[1], NM_012311.3:c.*1722CT[1]

Select item 14914025165.

rs1491402516 has merged into rs59238687 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAA>-,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:7767875 (GRCh38)
10:7809838 (GRCh37)
Canonical SPDI:: NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7767865:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
AAAA=0.000004/1 (TOPMED)
AAAAA=0.020089/9 (NorthernSweden)
HGVS:: NC_000010.11:g.7767875_7767884del, NC_000010.11:g.7767878_7767884del, NC_000010.11:g.7767879_7767884del, NC_000010.11:g.7767881_7767884del, NC_000010.11:g.7767882_7767884del, NC_000010.11:g.7767883_7767884del, NC_000010.11:g.7767884del, NC_000010.11:g.7767884dup, NC_000010.11:g.7767883_7767884dup, NC_000010.11:g.7767882_7767884dup, NC_000010.11:g.7767881_7767884dup, NC_000010.11:g.7767880_7767884dup, NC_000010.10:g.7809838_7809847del, NC_000010.10:g.7809841_7809847del, NC_000010.10:g.7809842_7809847del, NC_000010.10:g.7809844_7809847del, NC_000010.10:g.7809845_7809847del, NC_000010.10:g.7809846_7809847del, NC_000010.10:g.7809847del, NC_000010.10:g.7809847dup, NC_000010.10:g.7809846_7809847dup, NC_000010.10:g.7809845_7809847dup, NC_000010.10:g.7809844_7809847dup, NC_000010.10:g.7809843_7809847dup

Select item 14914015966.

rs1491401596 has merged into rs60757813 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,A,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:7777064 (GRCh38)
10:7819027 (GRCh37)
Canonical SPDI:: NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:7777053:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
-=0.2967/1486 (1000Genomes)
HGVS:: NC_000010.11:g.7777064_7777077del, NC_000010.11:g.7777065_7777077del, NC_000010.11:g.7777066_7777077del, NC_000010.11:g.7777068_7777077del, NC_000010.11:g.7777069_7777077del, NC_000010.11:g.7777070_7777077del, NC_000010.11:g.7777071_7777077del, NC_000010.11:g.7777072_7777077del, NC_000010.11:g.7777073_7777077del, NC_000010.11:g.7777074_7777077del, NC_000010.11:g.7777075_7777077del, NC_000010.11:g.7777076_7777077del, NC_000010.11:g.7777077del, NC_000010.11:g.7777077dup, NC_000010.11:g.7777076_7777077dup, NC_000010.11:g.7777075_7777077dup, NC_000010.11:g.7777074_7777077dup, NC_000010.11:g.7777073_7777077dup, NC_000010.11:g.7777072_7777077dup, NC_000010.11:g.7777071_7777077dup, NC_000010.11:g.7777070_7777077dup, NC_000010.11:g.7777069_7777077dup, NC_000010.11:g.7777063_7777077dup, NC_000010.11:g.7777059_7777077dup, NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.7777077_7777078insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.7819027_7819040del, NC_000010.10:g.7819028_7819040del, NC_000010.10:g.7819029_7819040del, NC_000010.10:g.7819031_7819040del, NC_000010.10:g.7819032_7819040del, NC_000010.10:g.7819033_7819040del, NC_000010.10:g.7819034_7819040del, NC_000010.10:g.7819035_7819040del, NC_000010.10:g.7819036_7819040del, NC_000010.10:g.7819037_7819040del, NC_000010.10:g.7819038_7819040del, NC_000010.10:g.7819039_7819040del, NC_000010.10:g.7819040del, NC_000010.10:g.7819040dup, NC_000010.10:g.7819039_7819040dup, NC_000010.10:g.7819038_7819040dup, NC_000010.10:g.7819037_7819040dup, NC_000010.10:g.7819036_7819040dup, NC_000010.10:g.7819035_7819040dup, NC_000010.10:g.7819034_7819040dup, NC_000010.10:g.7819033_7819040dup, NC_000010.10:g.7819032_7819040dup, NC_000010.10:g.7819026_7819040dup, NC_000010.10:g.7819022_7819040dup, NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.7819040_7819041insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14913567227.

rs1491356722 has merged into rs68002439 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAA>-,A,AA,AAAA,AAAAAAA [Show Flanks]
Chromosome:: 10:7785825 (GRCh38)
10:7827788 (GRCh37)
Canonical SPDI:: NC_000010.11:7785813:AAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:7785813:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:7785813:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:7785813:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7785813:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAA=0./0 (ALFA)
-=0.329253/87150 (TOPMED)
-=0.388889/224 (NorthernSweden)
HGVS:: NC_000010.11:g.7785825_7785827del, NC_000010.11:g.7785826_7785827del, NC_000010.11:g.7785827del, NC_000010.11:g.7785827dup, NC_000010.11:g.7785824_7785827dup, NC_000010.10:g.7827788_7827790del, NC_000010.10:g.7827789_7827790del, NC_000010.10:g.7827790del, NC_000010.10:g.7827790dup, NC_000010.10:g.7827787_7827790dup

Select item 14913080488.

rs1491308048 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:7777904 (GRCh38)
10:7819867 (GRCh37)
Canonical SPDI:: NC_000010.11:7777903:CA:
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000033/4 (GnomAD)
-=0.000212/4 (TOMMO)
-=0.010941/20 (Korea1K)
HGVS:: NC_000010.11:g.7777904_7777905del, NC_000010.10:g.7819867_7819868del

Select item 14912698629.

rs1491269862 has merged into rs148544006 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA [Show Flanks]
Chromosome:: 10:7777917 (GRCh38)
10:7819880 (GRCh37)
Canonical SPDI:: NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:7777904:AAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.7777917_7777918del, NC_000010.11:g.7777918del, NC_000010.11:g.7777918dup, NC_000010.11:g.7777917_7777918dup, NC_000010.11:g.7777916_7777918dup, NC_000010.11:g.7777915_7777918dup, NC_000010.11:g.7777914_7777918dup, NC_000010.10:g.7819880_7819881del, NC_000010.10:g.7819881del, NC_000010.10:g.7819881dup, NC_000010.10:g.7819880_7819881dup, NC_000010.10:g.7819879_7819881dup, NC_000010.10:g.7819878_7819881dup, NC_000010.10:g.7819877_7819881dup

Select item 149120580910.

rs1491205809 has merged into rs773686139 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 10:7785813 (GRCh38)
10:7827776 (GRCh37)
Canonical SPDI:: NC_000010.11:7785811:AGA:A
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000036/4 (GnomAD)
-=0.128641/477 (TWINSUK)
HGVS:: NC_000010.11:g.7785813_7785814del, NC_000010.10:g.7827776_7827777del

Select item 149110082811.

rs1491100828 has merged into rs34194283 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAA,AAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:7758684 (GRCh38)
10:7800647 (GRCh37)
Canonical SPDI:: NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:7758675:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.3478/1742 (1000Genomes)
HGVS:: NC_000010.11:g.7758684_7758691del, NC_000010.11:g.7758687_7758691del, NC_000010.11:g.7758688_7758691del, NC_000010.11:g.7758689_7758691del, NC_000010.11:g.7758690_7758691del, NC_000010.11:g.7758691del, NC_000010.11:g.7758691dup, NC_000010.11:g.7758688_7758691dup, NC_000010.10:g.7800647_7800654del, NC_000010.10:g.7800650_7800654del, NC_000010.10:g.7800651_7800654del, NC_000010.10:g.7800652_7800654del, NC_000010.10:g.7800653_7800654del, NC_000010.10:g.7800654del, NC_000010.10:g.7800654dup, NC_000010.10:g.7800651_7800654dup, XM_006717434.5:c.*1141_*1148del, XM_006717434.5:c.*1144_*1148del, XM_006717434.5:c.*1145_*1148del, XM_006717434.5:c.*1146_*1148del, XM_006717434.5:c.*1147_*1148del, XM_006717434.5:c.*1148del, XM_006717434.5:c.*1148dup, XM_006717434.5:c.*1145_*1148dup, XM_006717434.4:c.*1141_*1148del, XM_006717434.4:c.*1144_*1148del, XM_006717434.4:c.*1145_*1148del, XM_006717434.4:c.*1146_*1148del, XM_006717434.4:c.*1147_*1148del, XM_006717434.4:c.*1148del, XM_006717434.4:c.*1148dup, XM_006717434.4:c.*1145_*1148dup, XM_006717434.3:c.*1141_*1148del, XM_006717434.3:c.*1144_*1148del, XM_006717434.3:c.*1145_*1148del, XM_006717434.3:c.*1146_*1148del, XM_006717434.3:c.*1147_*1148del, XM_006717434.3:c.*1148del, XM_006717434.3:c.*1148dup, XM_006717434.3:c.*1145_*1148dup, XM_006717434.2:c.*1141_*1148del, XM_006717434.2:c.*1144_*1148del, XM_006717434.2:c.*1145_*1148del, XM_006717434.2:c.*1146_*1148del, XM_006717434.2:c.*1147_*1148del, XM_006717434.2:c.*1148del, XM_006717434.2:c.*1148dup, XM_006717434.2:c.*1145_*1148dup, XM_006717435.5:c.*1141_*1148del, XM_006717435.5:c.*1144_*1148del, XM_006717435.5:c.*1145_*1148del, XM_006717435.5:c.*1146_*1148del, XM_006717435.5:c.*1147_*1148del, XM_006717435.5:c.*1148del, XM_006717435.5:c.*1148dup, XM_006717435.5:c.*1145_*1148dup, XM_006717435.4:c.*1141_*1148del, XM_006717435.4:c.*1144_*1148del, XM_006717435.4:c.*1145_*1148del, XM_006717435.4:c.*1146_*1148del, XM_006717435.4:c.*1147_*1148del, XM_006717435.4:c.*1148del, XM_006717435.4:c.*1148dup, XM_006717435.4:c.*1145_*1148dup, XM_006717435.3:c.*1141_*1148del, XM_006717435.3:c.*1144_*1148del, XM_006717435.3:c.*1145_*1148del, XM_006717435.3:c.*1146_*1148del, XM_006717435.3:c.*1147_*1148del, XM_006717435.3:c.*1148del, XM_006717435.3:c.*1148dup, XM_006717435.3:c.*1145_*1148dup, XM_006717435.2:c.*1141_*1148del, XM_006717435.2:c.*1144_*1148del, XM_006717435.2:c.*1145_*1148del, XM_006717435.2:c.*1146_*1148del, XM_006717435.2:c.*1147_*1148del, XM_006717435.2:c.*1148del, XM_006717435.2:c.*1148dup, XM_006717435.2:c.*1145_*1148dup

Select item 149107270112.

rs1491072701 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 10:7776748 (GRCh38)
10:7818711 (GRCh37)
Canonical SPDI:: NC_000010.11:7776746:AGA:A
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000494/8 (ALFA)
-=0.001013/135 (GnomAD)
-=0.051043/93 (Korea1K)
HGVS:: NC_000010.11:g.7776748_7776749del, NC_000010.10:g.7818711_7818712del

Select item 149084991013.

rs1490849910 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:7774763 (GRCh38)
10:7816726 (GRCh37)
Canonical SPDI:: NC_000010.11:7774762:A:G
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.7774763A>G, NC_000010.10:g.7816726A>G

Select item 149077867514.

rs1490778675 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:7768130 (GRCh38)
10:7810094 (GRCh37)
Canonical SPDI:: NC_000010.11:7768130:A:AA
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000010.11:g.7768131dup, NC_000010.10:g.7810094dup

Select item 149067051615.

rs1490670516 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:7779105 (GRCh38)
10:7821068 (GRCh37)
Canonical SPDI:: NC_000010.11:7779104:C:G
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.7779105C>G, NC_000010.10:g.7821068C>G

Select item 149064594116.

rs1490645941 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:7777078 (GRCh38)
10:7819041 (GRCh37)
Canonical SPDI:: NC_000010.11:7777077:T:A
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.0087/142 (ALFA)
A=0.01507/44 (KOREAN)
A=0.01647/276 (TOMMO)
HGVS:: NC_000010.11:g.7777078T>A, NC_000010.10:g.7819041T>A

Select item 149037432617.

rs1490374326 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 10:7776229 (GRCh38)
10:7818192 (GRCh37)
Canonical SPDI:: NC_000010.11:7776228:C:
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.7776229del, NC_000010.10:g.7818192del

Select item 149035809818.

rs1490358098 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:7775225 (GRCh38)
10:7817188 (GRCh37)
Canonical SPDI:: NC_000010.11:7775224:T:C
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.7775225T>C, NC_000010.10:g.7817188T>C

Select item 149033570419.

rs1490335704 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:7758634 (GRCh38)
10:7800597 (GRCh37)
Canonical SPDI:: NC_000010.11:7758633:C:G,NC_000010.11:7758633:C:T
Gene:: KIN (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
HGVS:: NC_000010.11:g.7758634C>G, NC_000010.11:g.7758634C>T, NC_000010.10:g.7800597C>G, NC_000010.10:g.7800597C>T, XM_006717434.5:c.*1190G>C, XM_006717434.5:c.*1190G>A, XM_006717434.4:c.*1190G>C, XM_006717434.4:c.*1190G>A, XM_006717434.3:c.*1190G>C, XM_006717434.3:c.*1190G>A, XM_006717434.2:c.*1190G>C, XM_006717434.2:c.*1190G>A, XM_006717435.5:c.*1190G>C, XM_006717435.5:c.*1190G>A, XM_006717435.4:c.*1190G>C, XM_006717435.4:c.*1190G>A, XM_006717435.3:c.*1190G>C, XM_006717435.3:c.*1190G>A, XM_006717435.2:c.*1190G>C, XM_006717435.2:c.*1190G>A

Select item 149030056320.

rs1490300563 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:7782447 (GRCh38)
10:7824410 (GRCh37)
Canonical SPDI:: NC_000010.11:7782446:A:G
Gene:: KIN (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.7782447A>G, NC_000010.10:g.7824410A>G

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