SNP Links for Gene (Select 100128811) - SNP

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Select item 14914472171.

rs1491447217 has merged into rs55721545 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:25163177 (GRCh38)
10:25452106 (GRCh37)
Canonical SPDI:: NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:25163164:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.25163177_25163189del, NC_000010.11:g.25163180_25163189del, NC_000010.11:g.25163181_25163189del, NC_000010.11:g.25163182_25163189del, NC_000010.11:g.25163183_25163189del, NC_000010.11:g.25163184_25163189del, NC_000010.11:g.25163185_25163189del, NC_000010.11:g.25163186_25163189del, NC_000010.11:g.25163187_25163189del, NC_000010.11:g.25163188_25163189del, NC_000010.11:g.25163189del, NC_000010.11:g.25163189dup, NC_000010.11:g.25163188_25163189dup, NC_000010.11:g.25163187_25163189dup, NC_000010.11:g.25163186_25163189dup, NC_000010.11:g.25163185_25163189dup, NC_000010.11:g.25163184_25163189dup, NC_000010.11:g.25163183_25163189dup, NC_000010.11:g.25163182_25163189dup, NC_000010.11:g.25163181_25163189dup, NC_000010.11:g.25163180_25163189dup, NC_000010.11:g.25163179_25163189dup, NC_000010.11:g.25163178_25163189dup, NC_000010.11:g.25163177_25163189dup, NC_000010.11:g.25163170_25163189dup, NC_000010.11:g.25163169_25163189dup, NC_000010.10:g.25452106_25452118del, NC_000010.10:g.25452109_25452118del, NC_000010.10:g.25452110_25452118del, NC_000010.10:g.25452111_25452118del, NC_000010.10:g.25452112_25452118del, NC_000010.10:g.25452113_25452118del, NC_000010.10:g.25452114_25452118del, NC_000010.10:g.25452115_25452118del, NC_000010.10:g.25452116_25452118del, NC_000010.10:g.25452117_25452118del, NC_000010.10:g.25452118del, NC_000010.10:g.25452118dup, NC_000010.10:g.25452117_25452118dup, NC_000010.10:g.25452116_25452118dup, NC_000010.10:g.25452115_25452118dup, NC_000010.10:g.25452114_25452118dup, NC_000010.10:g.25452113_25452118dup, NC_000010.10:g.25452112_25452118dup, NC_000010.10:g.25452111_25452118dup, NC_000010.10:g.25452110_25452118dup, NC_000010.10:g.25452109_25452118dup, NC_000010.10:g.25452108_25452118dup, NC_000010.10:g.25452107_25452118dup, NC_000010.10:g.25452106_25452118dup, NC_000010.10:g.25452099_25452118dup, NC_000010.10:g.25452098_25452118dup

Select item 14913473432.

rs1491347343 [Homo sapiens]

Variant type:: INS
Alleles:: ->CAAA,CAAAA,G [Show Flanks]
Chromosome:: 10:25165460 (GRCh38)
10:25454390 (GRCh37)
Canonical SPDI:: NC_000010.11:25165460::CAAA,NC_000010.11:25165460::CAAAA,NC_000010.11:25165460::G
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.25165460_25165461insCAAA, NC_000010.11:g.25165460_25165461insCAAAA, NC_000010.11:g.25165460_25165461insG, NC_000010.10:g.25454389_25454390insCAAA, NC_000010.10:g.25454389_25454390insCAAAA, NC_000010.10:g.25454389_25454390insG

Select item 14913431583.

rs1491343158 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:25165460 (GRCh38)
10:25454389 (GRCh37)
Canonical SPDI:: NC_000010.11:25165459:CA:
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.25165460_25165461del, NC_000010.10:g.25454389_25454390del

Select item 14913385044.

rs1491338504 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:25163986 (GRCh38)
10:25452915 (GRCh37)
Canonical SPDI:: NC_000010.11:25163985:AT:
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00108/29 (TOMMO)
HGVS:: NC_000010.11:g.25163986_25163987del, NC_000010.10:g.25452915_25452916del

Select item 14912785105.

rs1491278510 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:25163164 (GRCh38)
10:25452093 (GRCh37)
Canonical SPDI:: NC_000010.11:25163163:CA:
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00025/3 (ALFA)
HGVS:: NC_000010.11:g.25163164_25163165del, NC_000010.10:g.25452093_25452094del

Select item 14911603836.

rs1491160383 has merged into rs375540159 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:25163997 (GRCh38)
10:25452926 (GRCh37)
Canonical SPDI:: NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:25163986:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTTTTTT=0.2143/1073 (1000Genomes)
HGVS:: NC_000010.11:g.25163997_25164015del, NC_000010.11:g.25163998_25164015del, NC_000010.11:g.25163999_25164015del, NC_000010.11:g.25164000_25164015del, NC_000010.11:g.25164001_25164015del, NC_000010.11:g.25164002_25164015del, NC_000010.11:g.25164003_25164015del, NC_000010.11:g.25164004_25164015del, NC_000010.11:g.25164005_25164015del, NC_000010.11:g.25164006_25164015del, NC_000010.11:g.25164007_25164015del, NC_000010.11:g.25164008_25164015del, NC_000010.11:g.25164009_25164015del, NC_000010.11:g.25164010_25164015del, NC_000010.11:g.25164011_25164015del, NC_000010.11:g.25164012_25164015del, NC_000010.11:g.25164013_25164015del, NC_000010.11:g.25164014_25164015del, NC_000010.11:g.25164015del, NC_000010.11:g.25164015dup, NC_000010.11:g.25164014_25164015dup, NC_000010.11:g.25164013_25164015dup, NC_000010.11:g.25164012_25164015dup, NC_000010.11:g.25164011_25164015dup, NC_000010.11:g.25164010_25164015dup, NC_000010.11:g.25164009_25164015dup, NC_000010.11:g.25164007_25164015dup, NC_000010.11:g.25164006_25164015dup, NC_000010.11:g.25164001_25164015dup, NC_000010.11:g.25163999_25164015dup, NC_000010.11:g.25163998_25164015dup, NC_000010.11:g.25163987_25164015T[50]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.11:g.25163990_25164015dup, NC_000010.11:g.25163987_25164015T[56]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.11:g.25164015_25164016insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.25452926_25452944del, NC_000010.10:g.25452927_25452944del, NC_000010.10:g.25452928_25452944del, NC_000010.10:g.25452929_25452944del, NC_000010.10:g.25452930_25452944del, NC_000010.10:g.25452931_25452944del, NC_000010.10:g.25452932_25452944del, NC_000010.10:g.25452933_25452944del, NC_000010.10:g.25452934_25452944del, NC_000010.10:g.25452935_25452944del, NC_000010.10:g.25452936_25452944del, NC_000010.10:g.25452937_25452944del, NC_000010.10:g.25452938_25452944del, NC_000010.10:g.25452939_25452944del, NC_000010.10:g.25452940_25452944del, NC_000010.10:g.25452941_25452944del, NC_000010.10:g.25452942_25452944del, NC_000010.10:g.25452943_25452944del, NC_000010.10:g.25452944del, NC_000010.10:g.25452944dup, NC_000010.10:g.25452943_25452944dup, NC_000010.10:g.25452942_25452944dup, NC_000010.10:g.25452941_25452944dup, NC_000010.10:g.25452940_25452944dup, NC_000010.10:g.25452939_25452944dup, NC_000010.10:g.25452938_25452944dup, NC_000010.10:g.25452936_25452944dup, NC_000010.10:g.25452935_25452944dup, NC_000010.10:g.25452930_25452944dup, NC_000010.10:g.25452928_25452944dup, NC_000010.10:g.25452927_25452944dup, NC_000010.10:g.25452916_25452944T[50]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.25452919_25452944dup, NC_000010.10:g.25452916_25452944T[56]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.25452944_25452945insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14910668767.

rs1491066876 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,AAA,AAAAA,AAAAAAAAA,GAAAAAA [Show Flanks]
Chromosome:: 10:25165459 (GRCh38)
10:25454389 (GRCh37)
Canonical SPDI:: NC_000010.11:25165459::A,NC_000010.11:25165459::AAA,NC_000010.11:25165459::AAAAA,NC_000010.11:25165459::AAAAAAAAA,NC_000010.11:25165459::GAAAAAA
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
AAAAA=0.00008/2 (TOMMO)
HGVS:: NC_000010.11:g.25165459_25165460insA, NC_000010.11:g.25165459_25165460insAAA, NC_000010.11:g.25165459_25165460insAAAAA, NC_000010.11:g.25165459_25165460insAAAAAAAAA, NC_000010.11:g.25165459_25165460insGAAAAAA, NC_000010.10:g.25454388_25454389insA, NC_000010.10:g.25454388_25454389insAAA, NC_000010.10:g.25454388_25454389insAAAAA, NC_000010.10:g.25454388_25454389insAAAAAAAAA, NC_000010.10:g.25454388_25454389insGAAAAAA

Select item 14908629728.

rs1490862972 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:25165529 (GRCh38)
10:25454458 (GRCh37)
Canonical SPDI:: NC_000010.11:25165528:G:A
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.25165529G>A, NC_000010.10:g.25454458G>A

Select item 14905324409.

rs1490532440 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:25174813 (GRCh38)
10:25463742 (GRCh37)
Canonical SPDI:: NC_000010.11:25174812:C:G,NC_000010.11:25174812:C:T
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.25174813C>G, NC_000010.11:g.25174813C>T, NC_000010.10:g.25463742C>G, NC_000010.10:g.25463742C>T

Select item 149037217010.

rs1490372170 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:25165146 (GRCh38)
10:25454075 (GRCh37)
Canonical SPDI:: NC_000010.11:25165145:T:C
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.25165146T>C, NC_000010.10:g.25454075T>C

Select item 149031376911.

rs1490313769 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:25173775 (GRCh38)
10:25462704 (GRCh37)
Canonical SPDI:: NC_000010.11:25173774:G:C
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.25173775G>C, NC_000010.10:g.25462704G>C

Select item 149028297312.

rs1490282973 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:25174800 (GRCh38)
10:25463729 (GRCh37)
Canonical SPDI:: NC_000010.11:25174799:C:T
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000023/6 (TOPMED)
T=0.000342/1 (KOREAN)
T=0.000558/1 (Korea1K)
HGVS:: NC_000010.11:g.25174800C>T, NC_000010.10:g.25463729C>T

Select item 149014934613.

rs1490149346 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:25171325 (GRCh38)
10:25460254 (GRCh37)
Canonical SPDI:: NC_000010.11:25171324:A:G
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.25171325A>G, NC_000010.10:g.25460254A>G

Select item 149004160914.

rs1490041609 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:25173805 (GRCh38)
10:25462734 (GRCh37)
Canonical SPDI:: NC_000010.11:25173804:G:A
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.25173805G>A, NC_000010.10:g.25462734G>A

Select item 148979352015.

rs1489793520 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:25174397 (GRCh38)
10:25463326 (GRCh37)
Canonical SPDI:: NC_000010.11:25174396:G:C
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.25174397G>C, NC_000010.10:g.25463326G>C

Select item 148974257316.

rs1489742573 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 10:25161567 (GRCh38)
10:25450496 (GRCh37)
Canonical SPDI:: NC_000010.11:25161566:AAAAA:AAAA
Gene:: GPR158-AS1 (Varview), LINC01516 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAA=0.000214/3 (ALFA)
-=0.000086/12 (GnomAD)
-=0.000087/23 (TOPMED)
HGVS:: NC_000010.11:g.25161571del, NC_000010.10:g.25450500del

Select item 148962050717.

rs1489620507 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 10:25166812 (GRCh38)
10:25455741 (GRCh37)
Canonical SPDI:: NC_000010.11:25166811:G:C,NC_000010.11:25166811:G:T
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.25166812G>C, NC_000010.11:g.25166812G>T, NC_000010.10:g.25455741G>C, NC_000010.10:g.25455741G>T

Select item 148921897618.

rs1489218976 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:25162936 (GRCh38)
10:25451865 (GRCh37)
Canonical SPDI:: NC_000010.11:25162935:T:G
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.25162936T>G, NC_000010.10:g.25451865T>G

Select item 148921743519.

rs1489217435 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:25174881 (GRCh38)
10:25463810 (GRCh37)
Canonical SPDI:: NC_000010.11:25174880:C:T
Gene:: GPR158 (Varview), GPR158-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.25174881C>T, NC_000010.10:g.25463810C>T

Select item 148910930420.

rs1489109304 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 10:25169688 (GRCh38)
10:25458617 (GRCh37)
Canonical SPDI:: NC_000010.11:25169687:T:A,NC_000010.11:25169687:T:C
Gene:: GPR158-AS1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000043/6 (GnomAD)
HGVS:: NC_000010.11:g.25169688T>A, NC_000010.11:g.25169688T>C, NC_000010.10:g.25458617T>A, NC_000010.10:g.25458617T>C

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