SNP Links for Gene (Select 102724250) - SNP

Links from Gene

Items: 1 to 20 of 67

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Select item 8792446931.

rs879244693 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: NT_187366.1:27409 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:27408:A:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NT_187366.1:g.27409A>C, NM_017940.5:c.206T>G, NM_017940.8:c.206T>G, NM_017940.7:c.206T>G, NM_017940.6:c.206T>G, NM_017940.4:c.206T>G, NM_001395905.1:c.206T>G, NM_001395905.2:c.206T>G, NM_001406552.1:c.1019C>T, NM_001406552.1:c.1019C>G, NP_001382834.1:p.Phe69Cys

Select item 8792442832.

rs879244283 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: NT_187366.1:26385 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:26384:T:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.26385T>C, NM_017940.5:c.399A>G, NM_017940.8:c.399G>A, NM_017940.7:c.399G>A, NM_017940.6:c.399G>A, NM_017940.4:c.399A>G, NM_001395905.1:c.399A>G, NM_001395905.2:c.399G>A, NM_001406552.1:c.1212G>A

Select item 8792358093.

rs879235809 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: NT_187366.1:8951 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8950:T:A,NT_187366.1:8950:T:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.8951T>A, NT_187366.1:g.8951T>G

Select item 8792171604.

rs879217160 has merged into rs71250813 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: NT_187366.1:8463 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8462:AAAA:AAA
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.8466del

Select item 8792112085.

rs879211208 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: NT_187366.1:19620 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:19619:G:A
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.19620G>A

Select item 8791958326.

rs879195832 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: NT_187366.1:8089 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8088:G:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
HGVS:: NT_187366.1:g.8089G>C

Select item 8791930847.

rs879193084 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_187366.1:21562 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:21561:C:T
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.21562C>T

Select item 8791898218.

rs879189821 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_187366.1:28026 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:28025:C:T
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
HGVS:: NT_187366.1:g.28026C>T

Select item 8791613259.

rs879161325 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: NT_187366.1:5974 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:5973:G:T
Gene:: LOC102724250 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.5974G>T, NM_017940.5:c.*153C>A, NM_017940.8:c.*153C>A, NM_017940.7:c.*153C>A, NM_017940.6:c.*153C>A, NM_017940.4:c.*153C>A, NM_001395905.1:c.*153C>A, NM_001395905.2:c.*153C>A, NM_001406552.1:c.*153C>A

Select item 87915578610.

rs879155786 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: NT_187366.1:18955 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:18954:G:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NT_187366.1:g.18955G>C, NM_017940.5:c.2134C>G, NM_017940.8:c.2134G>C, NM_017940.7:c.2134G>C, NM_017940.6:c.2134G>C, NM_017940.4:c.2134C>G, NM_001395905.1:c.1321C>G, NM_001395905.2:c.1321G>C, NM_001406552.1:c.2134G>C, NP_001382834.1:p.His441Asp

Select item 87915167711.

rs879151677 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: NT_187366.1:8975 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8974:T:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.8975T>C

Select item 87915041712.

rs879150417 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: NT_187366.1:8980 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8979:A:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
HGVS:: NT_187366.1:g.8980A>G

Select item 87914417713.

rs879144177 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: NT_187366.1:7663 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:7662:T:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.7663T>G

Select item 87914326214.

rs879143262 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: NT_187366.1:23430 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:23429:T:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.23430T>G

Select item 87913907915.

rs879139079 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: NT_187366.1:10572 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:10571:C:T
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
HGVS:: NT_187366.1:g.10572C>T

Select item 87913097216.

rs879130972 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: NT_187366.1:18652 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:18651:C:A,NT_187366.1:18651:C:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.18652C>A, NT_187366.1:g.18652C>G

Select item 87913092817.

rs879130928 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: NT_187366.1:27419 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:27418:G:C
Gene:: LOC102724250 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.27419G>C, NM_017940.5:c.196C>G, NM_017940.8:c.196C>G, NM_017940.7:c.196C>G, NM_017940.6:c.196C>G, NM_017940.4:c.196C>G, NM_001395905.1:c.196C>G, NM_001395905.2:c.196G>C, NM_001406552.1:c.1009C>G, NP_001382834.1:p.Leu66Val

Select item 87911694618.

rs879116946 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: NT_187366.1:27944 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:27943:T:G
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.27944T>G

Select item 87911629519.

rs879116295 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: NT_187366.1:23575 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:23574:G:A
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.23575G>A

Select item 87911373120.

rs879113731 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: NT_187366.1:8758 (GRCh38)
NT_187366.1:-1 (GRCh37)
Canonical SPDI:: NT_187366.1:8757:A:G,NT_187366.1:8757:A:T
Gene:: LOC102724250 (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NT_187366.1:g.8758A>G, NT_187366.1:g.8758A>T

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