SNP Links for Protein (Select 32698736) - SNP

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91382856 (GRCh38)
5:90678673 (GRCh37)
Canonical SPDI:: NC_000005.10:91382855:T:C
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant,synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.91382856T>C, NC_000005.9:g.90678673T>C, NG_051241.1:g.5518A>G, NM_020801.4:c.237A>G, NM_020801.3:c.237A>G, NM_020801.2:c.237A>G, NR_138072.2:n.462A>G, NR_138072.1:n.518A>G, NM_001329672.2:c.-276A>G, NM_001329672.1:c.-276A>G

Select item 14706132927.

rs1470613292 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91375589 (GRCh38)
5:90671406 (GRCh37)
Canonical SPDI:: NC_000005.10:91375588:T:C
Gene:: ARRDC3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.91375589T>C, NC_000005.9:g.90671406T>C, NG_051241.1:g.12785A>G, NM_020801.4:c.535A>G, NM_020801.3:c.535A>G, NM_020801.2:c.535A>G, NR_138071.2:n.905A>G, NR_138071.1:n.1105A>G, NM_001329670.2:c.-126A>G, NM_001329670.1:c.-126A>G, NR_138072.2:n.760A>G, NR_138072.1:n.816A>G, NM_001329671.2:c.-126A>G, NM_001329671.1:c.-126A>G, NM_001329672.2:c.-126A>G, NM_001329672.1:c.-126A>G, NP_065852.1:p.Lys179Glu

Select item 14657980648.

rs1465798064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:91382865 (GRCh38)
5:90678682 (GRCh37)
Canonical SPDI:: NC_000005.10:91382864:A:C
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,genic_upstream_transcript_variant,intron_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000447/2 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000446/2 (Estonian)
HGVS:: NC_000005.10:g.91382865A>C, NC_000005.9:g.90678682A>C, NG_051241.1:g.5509T>G, NM_020801.4:c.228T>G, NM_020801.3:c.228T>G, NM_020801.2:c.228T>G, NR_138072.2:n.453T>G, NR_138072.1:n.509T>G, NM_001329672.2:c.-285T>G, NM_001329672.1:c.-285T>G

Select item 14633325499.

rs1463332549 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:91375610 (GRCh38)
5:90671427 (GRCh37)
Canonical SPDI:: NC_000005.10:91375609:G:T
Gene:: ARRDC3 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.91375610G>T, NC_000005.9:g.90671427G>T, NG_051241.1:g.12764C>A, NM_020801.4:c.514C>A, NM_020801.3:c.514C>A, NM_020801.2:c.514C>A, NR_138071.2:n.884C>A, NR_138071.1:n.1084C>A, NM_001329670.2:c.-147C>A, NM_001329670.1:c.-147C>A, NR_138072.2:n.739C>A, NR_138072.1:n.795C>A, NM_001329671.2:c.-147C>A, NM_001329671.1:c.-147C>A, NM_001329672.2:c.-147C>A, NM_001329672.1:c.-147C>A, NP_065852.1:p.Pro172Thr

Select item 146176248810.

rs1461762488 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91374925 (GRCh38)
5:90670742 (GRCh37)
Canonical SPDI:: NC_000005.10:91374924:T:C
Gene:: ARRDC3 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.91374925T>C, NC_000005.9:g.90670742T>C, NG_051241.1:g.13449A>G, NM_020801.4:c.867A>G, NM_020801.3:c.867A>G, NM_020801.2:c.867A>G, NR_138071.2:n.1237A>G, NR_138071.1:n.1437A>G, NM_001329670.2:c.207A>G, NM_001329670.1:c.207A>G, NR_138072.2:n.1092A>G, NR_138072.1:n.1148A>G, NM_001329671.2:c.207A>G, NM_001329671.1:c.207A>G, NM_001329672.2:c.207A>G, NM_001329672.1:c.207A>G

Select item 146021300111.

rs1460213001 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91373790 (GRCh38)
5:90669607 (GRCh37)
Canonical SPDI:: NC_000005.10:91373789:T:C
Gene:: ARRDC3 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.91373790T>C, NC_000005.9:g.90669607T>C, NG_051241.1:g.14584A>G, NM_020801.4:c.1082A>G, NM_020801.3:c.1082A>G, NM_020801.2:c.1082A>G, NR_138071.2:n.1490A>G, NR_138071.1:n.1690A>G, NM_001329670.2:c.422A>G, NM_001329670.1:c.422A>G, NR_138072.2:n.1345A>G, NR_138072.1:n.1401A>G, NM_001329671.2:c.422A>G, NM_001329671.1:c.422A>G, NM_001329672.2:c.422A>G, NM_001329672.1:c.422A>G, NP_065852.1:p.Asn361Ser, NP_001316599.1:p.Asn141Ser, NP_001316600.1:p.Asn141Ser, NP_001316601.1:p.Asn141Ser

Select item 145948880412.

rs1459488804 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:91376669 (GRCh38)
5:90672486 (GRCh37)
Canonical SPDI:: NC_000005.10:91376668:C:G
Gene:: ARRDC3 (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,intron_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000005.10:g.91376669C>G, NC_000005.9:g.90672486C>G, NG_051241.1:g.11705G>C, NM_020801.4:c.462G>C, NM_020801.3:c.462G>C, NM_020801.2:c.462G>C, NR_138071.2:n.832G>C, NR_138071.1:n.1032G>C, NM_001329670.2:c.-199G>C, NM_001329670.1:c.-199G>C, NR_138072.2:n.687G>C, NR_138072.1:n.743G>C, NP_065852.1:p.Lys154Asn

Select item 145521882113.

rs1455218821 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:91382924 (GRCh38)
5:90678741 (GRCh37)
Canonical SPDI:: NC_000005.10:91382923:C:T
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,5_prime_UTR_variant,coding_sequence_variant,genic_upstream_transcript_variant,missense_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_000005.10:g.91382924C>T, NC_000005.9:g.90678741C>T, NG_051241.1:g.5450G>A, NM_020801.4:c.169G>A, NM_020801.3:c.169G>A, NM_020801.2:c.169G>A, NR_138072.2:n.394G>A, NR_138072.1:n.450G>A, NM_001329672.2:c.-344G>A, NM_001329672.1:c.-344G>A, NP_065852.1:p.Val57Ile

Select item 145512145114.

rs1455121451 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 5:91374162 (GRCh38)
5:90669979 (GRCh37)
Canonical SPDI:: NC_000005.10:91374161:T:A,NC_000005.10:91374161:T:C
Gene:: ARRDC3 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000005.10:g.91374162T>A, NC_000005.10:g.91374162T>C, NC_000005.9:g.90669979T>A, NC_000005.9:g.90669979T>C, NG_051241.1:g.14212A>T, NG_051241.1:g.14212A>G, NM_020801.4:c.985A>T, NM_020801.4:c.985A>G, NM_020801.3:c.985A>T, NM_020801.3:c.985A>G, NM_020801.2:c.985A>T, NM_020801.2:c.985A>G, NR_138071.2:n.1355A>T, NR_138071.2:n.1355A>G, NR_138071.1:n.1555A>T, NR_138071.1:n.1555A>G, NM_001329670.2:c.325A>T, NM_001329670.2:c.325A>G, NM_001329670.1:c.325A>T, NM_001329670.1:c.325A>G, NR_138072.2:n.1210A>T, NR_138072.2:n.1210A>G, NR_138072.1:n.1266A>T, NR_138072.1:n.1266A>G, NM_001329671.2:c.325A>T, NM_001329671.2:c.325A>G, NM_001329671.1:c.325A>T, NM_001329671.1:c.325A>G, NM_001329672.2:c.325A>T, NM_001329672.2:c.325A>G, NM_001329672.1:c.325A>T, NM_001329672.1:c.325A>G, NP_065852.1:p.Ser329Cys, NP_065852.1:p.Ser329Gly, NP_001316599.1:p.Ser109Cys, NP_001316599.1:p.Ser109Gly, NP_001316600.1:p.Ser109Cys, NP_001316600.1:p.Ser109Gly, NP_001316601.1:p.Ser109Cys, NP_001316601.1:p.Ser109Gly

Select item 145101051415.

rs1451010514 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 5:91375560 (GRCh38)
5:90671377 (GRCh37)
Canonical SPDI:: NC_000005.10:91375559:T:C,NC_000005.10:91375559:T:G
Gene:: ARRDC3 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant,5_prime_UTR_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000005.10:g.91375560T>C, NC_000005.10:g.91375560T>G, NC_000005.9:g.90671377T>C, NC_000005.9:g.90671377T>G, NG_051241.1:g.12814A>G, NG_051241.1:g.12814A>C, NM_020801.4:c.564A>G, NM_020801.4:c.564A>C, NM_020801.3:c.564A>G, NM_020801.3:c.564A>C, NM_020801.2:c.564A>G, NM_020801.2:c.564A>C, NR_138071.2:n.934A>G, NR_138071.2:n.934A>C, NR_138071.1:n.1134A>G, NR_138071.1:n.1134A>C, NM_001329670.2:c.-97A>G, NM_001329670.2:c.-97A>C, NM_001329670.1:c.-97A>G, NM_001329670.1:c.-97A>C, NR_138072.2:n.789A>G, NR_138072.2:n.789A>C, NR_138072.1:n.845A>G, NR_138072.1:n.845A>C, NM_001329671.2:c.-97A>G, NM_001329671.2:c.-97A>C, NM_001329671.1:c.-97A>G, NM_001329671.1:c.-97A>C, NM_001329672.2:c.-97A>G, NM_001329672.2:c.-97A>C, NM_001329672.1:c.-97A>G, NM_001329672.1:c.-97A>C

Select item 144762515216.

rs1447625152 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 5:91375125 (GRCh38)
5:90670942 (GRCh37)
Canonical SPDI:: NC_000005.10:91375124:C:G,NC_000005.10:91375124:C:T
Gene:: ARRDC3 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000047/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.91375125C>G, NC_000005.10:g.91375125C>T, NC_000005.9:g.90670942C>G, NC_000005.9:g.90670942C>T, NG_051241.1:g.13249G>C, NG_051241.1:g.13249G>A, NM_020801.4:c.667G>C, NM_020801.4:c.667G>A, NM_020801.3:c.667G>C, NM_020801.3:c.667G>A, NM_020801.2:c.667G>C, NM_020801.2:c.667G>A, NR_138071.2:n.1037G>C, NR_138071.2:n.1037G>A, NR_138071.1:n.1237G>C, NR_138071.1:n.1237G>A, NM_001329670.2:c.7G>C, NM_001329670.2:c.7G>A, NM_001329670.1:c.7G>C, NM_001329670.1:c.7G>A, NR_138072.2:n.892G>C, NR_138072.2:n.892G>A, NR_138072.1:n.948G>C, NR_138072.1:n.948G>A, NM_001329671.2:c.7G>C, NM_001329671.2:c.7G>A, NM_001329671.1:c.7G>C, NM_001329671.1:c.7G>A, NM_001329672.2:c.7G>C, NM_001329672.2:c.7G>A, NM_001329672.1:c.7G>C, NM_001329672.1:c.7G>A, NP_065852.1:p.Val223Leu, NP_065852.1:p.Val223Met, NP_001316599.1:p.Val3Leu, NP_001316599.1:p.Val3Met, NP_001316600.1:p.Val3Leu, NP_001316600.1:p.Val3Met, NP_001316601.1:p.Val3Leu, NP_001316601.1:p.Val3Met

Select item 144268363117.

rs1442683631 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:91382857 (GRCh38)
5:90678674 (GRCh37)
Canonical SPDI:: NC_000005.10:91382856:A:G
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant,5_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.91382857A>G, NC_000005.9:g.90678674A>G, NG_051241.1:g.5517T>C, NM_020801.4:c.236T>C, NM_020801.3:c.236T>C, NM_020801.2:c.236T>C, NR_138072.2:n.461T>C, NR_138072.1:n.517T>C, NM_001329672.2:c.-277T>C, NM_001329672.1:c.-277T>C, NP_065852.1:p.Val79Ala

Select item 143838287118.

rs1438382871 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91373757 (GRCh38)
5:90669574 (GRCh37)
Canonical SPDI:: NC_000005.10:91373756:T:C
Gene:: ARRDC3 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.91373757T>C, NC_000005.9:g.90669574T>C, NG_051241.1:g.14617A>G, NM_020801.4:c.1115A>G, NM_020801.3:c.1115A>G, NM_020801.2:c.1115A>G, NR_138071.2:n.1523A>G, NR_138071.1:n.1723A>G, NM_001329670.2:c.455A>G, NM_001329670.1:c.455A>G, NR_138072.2:n.1378A>G, NR_138072.1:n.1434A>G, NM_001329671.2:c.455A>G, NM_001329671.1:c.455A>G, NM_001329672.2:c.455A>G, NM_001329672.1:c.455A>G, NP_065852.1:p.Glu372Gly, NP_001316599.1:p.Glu152Gly, NP_001316600.1:p.Glu152Gly, NP_001316601.1:p.Glu152Gly

Select item 143222454119.

rs1432224541 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91382978 (GRCh38)
5:90678795 (GRCh37)
Canonical SPDI:: NC_000005.10:91382977:T:C
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000031/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.91382978T>C, NC_000005.9:g.90678795T>C, NG_051241.1:g.5396A>G, NM_020801.4:c.115A>G, NM_020801.3:c.115A>G, NM_020801.2:c.115A>G, NR_138072.2:n.340A>G, NR_138072.1:n.396A>G, NM_001329672.2:c.-398A>G, NM_001329672.1:c.-398A>G, NP_065852.1:p.Thr39Ala

Select item 143052309120.

rs1430523091 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:91382906 (GRCh38)
5:90678723 (GRCh37)
Canonical SPDI:: NC_000005.10:91382905:T:C
Gene:: ARRDC3 (Varview), ARRDC3-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant,intron_variant,genic_upstream_transcript_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_000005.10:g.91382906T>C, NC_000005.9:g.90678723T>C, NG_051241.1:g.5468A>G, NM_020801.4:c.187A>G, NM_020801.3:c.187A>G, NM_020801.2:c.187A>G, NR_138072.2:n.412A>G, NR_138072.1:n.468A>G, NM_001329672.2:c.-326A>G, NM_001329672.1:c.-326A>G, NP_065852.1:p.Arg63Gly

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