SNP Links for Protein (Select 66472920) - SNP

Links from Protein

Items: 1 to 20 of 182

<< First< Prev

Page of 10

Next >Last >>

Select item 14843661281.

rs1484366128 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 13:43107246 (GRCh38)
13:43681382 (GRCh37)
Canonical SPDI:: NC_000013.11:43107245:T:C,NC_000013.11:43107245:T:G
Gene:: DNAJC15 (Varview)
Functional Consequence:: stop_lost,terminator_codon_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000013.11:g.43107246T>C, NC_000013.11:g.43107246T>G, NC_000013.10:g.43681382T>C, NC_000013.10:g.43681382T>G, NM_013238.3:c.451T>C, NM_013238.3:c.451T>G, NM_013238.2:c.451T>C, NM_013238.2:c.451T>G, NP_037370.2:p.Ter151Arg, NP_037370.2:p.Ter151Gly

Select item 14836373802.

rs1483637380 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:43107242 (GRCh38)
13:43681378 (GRCh37)
Canonical SPDI:: NC_000013.11:43107241:A:C
Gene:: DNAJC15 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000013.11:g.43107242A>C, NC_000013.10:g.43681378A>C, NM_013238.3:c.447A>C, NM_013238.2:c.447A>C, NP_037370.2:p.Lys149Asn

Select item 14803082613.

rs1480308261 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:43107227 (GRCh38)
13:43681363 (GRCh37)
Canonical SPDI:: NC_000013.11:43107226:A:G
Gene:: DNAJC15 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0.000028/1 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.43107227A>G, NC_000013.10:g.43681363A>G, NM_013238.3:c.432A>G, NM_013238.2:c.432A>G

Select item 14772331004.

rs1477233100 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:43068999 (GRCh38)
13:43643135 (GRCh37)
Canonical SPDI:: NC_000013.11:43068998:C:T
Gene:: DNAJC15 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43068999C>T, NC_000013.10:g.43643135C>T, NM_013238.3:c.230C>T, NM_013238.2:c.230C>T, NP_037370.2:p.Thr77Ile

Select item 14634596885.

rs1463459688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:43023695 (GRCh38)
13:43597831 (GRCh37)
Canonical SPDI:: NC_000013.11:43023694:G:C
Gene:: DNAJC15 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43023695G>C, NC_000013.10:g.43597831G>C, NM_013238.3:c.69G>C, NM_013238.2:c.69G>C

Select item 14601808666.

rs1460180866 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:43107198 (GRCh38)
13:43681334 (GRCh37)
Canonical SPDI:: NC_000013.11:43107197:G:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.43107198G>A, NC_000013.10:g.43681334G>A, NM_013238.3:c.403G>A, NM_013238.2:c.403G>A, NP_037370.2:p.Ala135Thr

Select item 14570787457.

rs1457078745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:43085779 (GRCh38)
13:43659915 (GRCh37)
Canonical SPDI:: NC_000013.11:43085778:G:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43085779G>A, NC_000013.10:g.43659915G>A, NM_013238.3:c.323G>A, NM_013238.2:c.323G>A, NP_037370.2:p.Gly108Asp

Select item 14422213448.

rs1442221344 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:43085811 (GRCh38)
13:43659947 (GRCh37)
Canonical SPDI:: NC_000013.11:43085810:G:C
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.43085811G>C, NC_000013.10:g.43659947G>C, NM_013238.3:c.355G>C, NM_013238.2:c.355G>C, NP_037370.2:p.Val119Leu

Select item 14419354239.

rs1441935423 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:43023638 (GRCh38)
13:43597774 (GRCh37)
Canonical SPDI:: NC_000013.11:43023637:T:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.43023638T>A, NC_000013.10:g.43597774T>A, NM_013238.3:c.12T>A, NM_013238.2:c.12T>A

Select item 143805363010.

rs1438053630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:43078634 (GRCh38)
13:43652770 (GRCh37)
Canonical SPDI:: NC_000013.11:43078633:G:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43078634G>A, NC_000013.10:g.43652770G>A, NM_013238.3:c.257G>A, NM_013238.2:c.257G>A, NP_037370.2:p.Gly86Glu

Select item 143419019411.

rs1434190194 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:43068949 (GRCh38)
13:43643085 (GRCh37)
Canonical SPDI:: NC_000013.11:43068948:C:T
Gene:: DNAJC15 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.43068949C>T, NC_000013.10:g.43643085C>T, NM_013238.3:c.180C>T, NM_013238.2:c.180C>T

Select item 142966649512.

rs1429666495 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:43078619 (GRCh38)
13:43652755 (GRCh37)
Canonical SPDI:: NC_000013.11:43078618:C:T
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000013.11:g.43078619C>T, NC_000013.10:g.43652755C>T, NM_013238.3:c.242C>T, NM_013238.2:c.242C>T, NP_037370.2:p.Ser81Leu

Select item 142913826513.

rs1429138265 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:43023688 (GRCh38)
13:43597824 (GRCh37)
Canonical SPDI:: NC_000013.11:43023687:A:G
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000013.11:g.43023688A>G, NC_000013.10:g.43597824A>G, NM_013238.3:c.62A>G, NM_013238.2:c.62A>G, NP_037370.2:p.Gln21Arg

Select item 142790313814.

rs1427903138 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:43107229 (GRCh38)
13:43681365 (GRCh37)
Canonical SPDI:: NC_000013.11:43107228:A:G
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.43107229A>G, NC_000013.10:g.43681365A>G, NM_013238.3:c.434A>G, NM_013238.2:c.434A>G, NP_037370.2:p.Glu145Gly

Select item 142380527815.

rs1423805278 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 13:43068940 (GRCh38)
13:43643076 (GRCh37)
Canonical SPDI:: NC_000013.11:43068939:A:G,NC_000013.11:43068939:A:T
Gene:: DNAJC15 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
T=0.000106/2 (TOMMO)
HGVS:: NC_000013.11:g.43068940A>G, NC_000013.11:g.43068940A>T, NC_000013.10:g.43643076A>G, NC_000013.10:g.43643076A>T, NM_013238.3:c.171A>G, NM_013238.3:c.171A>T, NM_013238.2:c.171A>G, NM_013238.2:c.171A>T

Select item 141570067216.

rs1415700672 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:43107186 (GRCh38)
13:43681322 (GRCh37)
Canonical SPDI:: NC_000013.11:43107185:C:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000013/3 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43107186C>A, NC_000013.10:g.43681322C>A, NM_013238.3:c.391C>A, NM_013238.2:c.391C>A, NP_037370.2:p.Pro131Thr

Select item 141348797517.

rs1413487975 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 13:43085838 (GRCh38)
13:43659974 (GRCh37)
Canonical SPDI:: NC_000013.11:43085837:G:A,NC_000013.11:43085837:G:C
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.43085838G>A, NC_000013.11:g.43085838G>C, NC_000013.10:g.43659974G>A, NC_000013.10:g.43659974G>C, NM_013238.3:c.382G>A, NM_013238.3:c.382G>C, NM_013238.2:c.382G>A, NM_013238.2:c.382G>C, NP_037370.2:p.Gly128Ser, NP_037370.2:p.Gly128Arg

Select item 141011037318.

rs1410110373 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:43065714 (GRCh38)
13:43639850 (GRCh37)
Canonical SPDI:: NC_000013.11:43065713:G:T
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.43065714G>T, NC_000013.10:g.43639850G>T, NM_013238.3:c.137G>T, NM_013238.2:c.137G>T, NP_037370.2:p.Gly46Val

Select item 140511041619.

rs1405110416 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:43107184 (GRCh38)
13:43681320 (GRCh37)
Canonical SPDI:: NC_000013.11:43107183:C:A
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.43107184C>A, NC_000013.10:g.43681320C>A, NM_013238.3:c.389C>A, NM_013238.2:c.389C>A, NP_037370.2:p.Ser130Tyr

Select item 140310393720.

rs1403103937 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:43078652 (GRCh38)
13:43652788 (GRCh37)
Canonical SPDI:: NC_000013.11:43078651:T:C
Gene:: DNAJC15 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.43078652T>C, NC_000013.10:g.43652788T>C, NM_013238.3:c.275T>C, NM_013238.2:c.275T>C, NP_037370.2:p.Met92Thr

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 182

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity