SNP Links for Gene (Select 2834) - SNP

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Select item 14907950111.

rs1490795011 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:118595593 (GRCh38)
10:120355105 (GRCh37)
Canonical SPDI:: NC_000010.11:118595592:C:T
Gene:: PRLHR (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.118595593C>T, NC_000010.10:g.120355105C>T, NM_004248.3:c.-84G>A, NM_004248.2:c.-84G>A

Select item 14892466222.

rs1489246622 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:118593045 (GRCh38)
10:120352557 (GRCh37)
Canonical SPDI:: NC_000010.11:118593044:G:T
Gene:: PRLHR (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.118593045G>T, NC_000010.10:g.120352557G>T, NM_004248.3:c.*1087C>A

Select item 14872460713.

rs1487246071 [Homo sapiens]

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

Select item 14871942884.

rs1487194288 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:118595562 (GRCh38)
10:120355074 (GRCh37)
Canonical SPDI:: NC_000010.11:118595561:G:A
Gene:: PRLHR (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
A=0.000177/3 (TOMMO)
HGVS:: NC_000010.11:g.118595562G>A, NC_000010.10:g.120355074G>A, NM_004248.3:c.-53C>T, NM_004248.2:c.-53C>T

Select item 14868680105.

rs1486868010 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:118594663 (GRCh38)
10:120354175 (GRCh37)
Canonical SPDI:: NC_000010.11:118594662:G:A,NC_000010.11:118594662:G:C
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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.118594663G>A, NC_000010.11:g.118594663G>C, NC_000010.10:g.120354175G>A, NC_000010.10:g.120354175G>C, NM_004248.3:c.582C>T, NM_004248.3:c.582C>G, NM_004248.2:c.582C>T, NM_004248.2:c.582C>G, NM_005287.1:c.579C>T, NM_005287.1:c.579C>G

Select item 14863918936.

rs1486391893 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:118594598 (GRCh38)
10:120354110 (GRCh37)
Canonical SPDI:: NC_000010.11:118594597:C:T
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000006/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.118594598C>T, NC_000010.10:g.120354110C>T, NM_004248.3:c.647G>A, NM_004248.2:c.647G>A, NM_005287.1:c.644G>A, NP_004239.2:p.Gly216Asp

Select item 14863259797.

rs1486325979 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:118594933 (GRCh38)
10:120354445 (GRCh37)
Canonical SPDI:: NC_000010.11:118594932:C:T
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.118594933C>T, NC_000010.10:g.120354445C>T, NM_004248.3:c.312G>A, NM_004248.2:c.312G>A, NM_005287.1:c.312G>A

Select item 14860499568.

rs1486049956 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:118595773 (GRCh38)
10:120355285 (GRCh37)
Canonical SPDI:: NC_000010.11:118595772:G:A,NC_000010.11:118595772:G:C
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000035/1 (TOMMO)
A=0.000036/5 (GnomAD)
HGVS:: NC_000010.11:g.118595773G>A, NC_000010.11:g.118595773G>C, NC_000010.10:g.120355285G>A, NC_000010.10:g.120355285G>C

Select item 14854458449.

rs1485445844 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 10:118595974 (GRCh38)
10:120355486 (GRCh37)
Canonical SPDI:: NC_000010.11:118595973:T:A,NC_000010.11:118595973:T:C
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.118595974T>A, NC_000010.11:g.118595974T>C, NC_000010.10:g.120355486T>A, NC_000010.10:g.120355486T>C

Select item 148538609410.

rs1485386094 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 10:118596806 (GRCh38)
10:120356318 (GRCh37)
Canonical SPDI:: NC_000010.11:118596805:A:C,NC_000010.11:118596805:A:G
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.118596806A>C, NC_000010.11:g.118596806A>G, NC_000010.10:g.120356318A>C, NC_000010.10:g.120356318A>G

Select item 148523040211.

rs1485230402 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:118595051 (GRCh38)
10:120354563 (GRCh37)
Canonical SPDI:: NC_000010.11:118595050:A:G
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,missense_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.118595051A>G, NC_000010.10:g.120354563A>G, NM_004248.3:c.194T>C, NM_004248.2:c.194T>C, NM_005287.1:c.194T>C, NP_004239.2:p.Leu65Pro

Select item 148514479812.

rs1485144798 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:118596890 (GRCh38)
10:120356402 (GRCh37)
Canonical SPDI:: NC_000010.11:118596889:T:C
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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.118596890T>C, NC_000010.10:g.120356402T>C

Select item 148451079313.

rs1484510793 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 10:118593911 (GRCh38)
10:120353424 (GRCh37)
Canonical SPDI:: NC_000010.11:118593911:CCCCC:CCCCCC
Gene:: PRLHR (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: CCCCCC=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.118593916dup, NC_000010.10:g.120353428dup, NM_004248.3:c.*220dup, NM_004248.2:c.*220dup

Select item 148311823614.

rs1483118236 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 10:118595060 (GRCh38)
10:120354572 (GRCh37)
Canonical SPDI:: NC_000010.11:118595059:A:G,NC_000010.11:118595059:A:T
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.118595060A>G, NC_000010.11:g.118595060A>T, NC_000010.10:g.120354572A>G, NC_000010.10:g.120354572A>T, NM_004248.3:c.185T>C, NM_004248.3:c.185T>A, NM_004248.2:c.185T>C, NM_004248.2:c.185T>A, NM_005287.1:c.185T>C, NM_005287.1:c.185T>A, NP_004239.2:p.Leu62Pro, NP_004239.2:p.Leu62Gln

Select item 148289069815.

rs1482890698 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:118595978 (GRCh38)
10:120355490 (GRCh37)
Canonical SPDI:: NC_000010.11:118595977:G:A
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.118595978G>A, NC_000010.10:g.120355490G>A

Select item 148277780416.

rs1482777804 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:118593557 (GRCh38)
10:120353069 (GRCh37)
Canonical SPDI:: NC_000010.11:118593556:G:A
Gene:: PRLHR (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000049/13 (TOPMED)
A=0.000086/12 (GnomAD)
HGVS:: NC_000010.11:g.118593557G>A, NC_000010.10:g.120353069G>A, NM_004248.3:c.*575C>T, NM_004248.2:c.*575C>T

Select item 148184283917.

rs1481842839 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:118597162 (GRCh38)
10:120356674 (GRCh37)
Canonical SPDI:: NC_000010.11:118597161:T:C
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.118597162T>C, NC_000010.10:g.120356674T>C

Select item 148095392718.

rs1480953927 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:118594926 (GRCh38)
10:120354438 (GRCh37)
Canonical SPDI:: NC_000010.11:118594925:C:T
Gene:: PRLHR (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000026/7 (TOPMED)
HGVS:: NC_000010.11:g.118594926C>T, NC_000010.10:g.120354438C>T, NM_004248.3:c.319G>A, NM_004248.2:c.319G>A, NM_005287.1:c.319G>A, NP_004239.2:p.Val107Met

Select item 148094962919.

rs1480949629 [Homo sapiens]

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

Select item 148084088820.

rs1480840888 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:118595911 (GRCh38)
10:120355423 (GRCh37)
Canonical SPDI:: NC_000010.11:118595910:G:A
Gene:: PRLHR (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.118595911G>A, NC_000010.10:g.120355423G>A

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