SNP Links for Protein (Select 126365761) - SNP

Links from Protein

Items: 1 to 20 of 750

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Select item 14906700661.

rs1490670066 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:65153435 (GRCh38)
17:63149553 (GRCh37)
Canonical SPDI:: NC_000017.11:65153434:T:C
Gene:: RGS9 (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_000017.11:g.65153435T>C, NC_000017.10:g.63149553T>C, NG_013021.2:g.21098T>C, NM_003835.4:c.71T>C, NM_003835.3:c.71T>C, NM_001081955.3:c.71T>C, NM_001081955.2:c.71T>C, NM_001165933.2:c.71T>C, NM_001165933.1:c.71T>C, NP_003826.2:p.Val24Ala, NP_001075424.1:p.Val24Ala, NP_001159405.1:p.Val24Ala

Select item 14883097342.

rs1488309734 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 17:65163015 (GRCh38)
17:63159133 (GRCh37)
Canonical SPDI:: NC_000017.11:65163014:A:T
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000031/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.65163015A>T, NC_000017.10:g.63159133A>T, NG_013021.2:g.30678A>T, NM_003835.4:c.426A>T, NM_003835.3:c.426A>T, NM_001081955.3:c.426A>T, NM_001081955.2:c.426A>T, NM_001165933.2:c.426A>T, NM_001165933.1:c.426A>T, NP_003826.2:p.Glu142Asp, NP_001075424.1:p.Glu142Asp, NP_001159405.1:p.Glu142Asp

Select item 14881333173.

rs1488133317 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:65168261 (GRCh38)
17:63164379 (GRCh37)
Canonical SPDI:: NC_000017.11:65168260:T:C,NC_000017.11:65168260:T:G
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.65168261T>C, NC_000017.11:g.65168261T>G, NC_000017.10:g.63164379T>C, NC_000017.10:g.63164379T>G, NG_013021.2:g.35924T>C, NG_013021.2:g.35924T>G, NM_003835.4:c.562T>C, NM_003835.4:c.562T>G, NM_003835.3:c.562T>C, NM_003835.3:c.562T>G, NM_001081955.3:c.562T>C, NM_001081955.3:c.562T>G, NM_001081955.2:c.562T>C, NM_001081955.2:c.562T>G, NM_001165933.2:c.562T>C, NM_001165933.2:c.562T>G, NM_001165933.1:c.562T>C, NM_001165933.1:c.562T>G, NP_003826.2:p.Trp188Arg, NP_003826.2:p.Trp188Gly, NP_001075424.1:p.Trp188Arg, NP_001075424.1:p.Trp188Gly, NP_001159405.1:p.Trp188Arg, NP_001159405.1:p.Trp188Gly

Select item 14877431714.

rs1487743171 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:65193610 (GRCh38)
17:63189728 (GRCh37)
Canonical SPDI:: NC_000017.11:65193609:C:G
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000017.11:g.65193610C>G, NC_000017.10:g.63189728C>G, NG_013021.2:g.61273C>G, NM_003835.4:c.814C>G, NM_003835.3:c.814C>G, NM_001081955.3:c.805C>G, NM_001081955.2:c.805C>G, NM_001165933.2:c.805C>G, NM_001165933.1:c.805C>G, NP_003826.2:p.Pro272Ala, NP_001075424.1:p.Pro269Ala, NP_001159405.1:p.Pro269Ala

Select item 14874734905.

rs1487473490 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:65207984 (GRCh38)
17:63204102 (GRCh37)
Canonical SPDI:: NC_000017.11:65207983:A:G
Gene:: RGS9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65207984A>G, NC_000017.10:g.63204102A>G, NG_013021.2:g.75647A>G, NM_003835.4:c.1266A>G, NM_003835.3:c.1266A>G, NM_001081955.3:c.1257A>G, NM_001081955.2:c.1257A>G, NM_001165933.2:c.1257A>G, NM_001165933.1:c.1257A>G

Select item 14863694776.

rs1486369477 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:65193593 (GRCh38)
17:63189711 (GRCh37)
Canonical SPDI:: NC_000017.11:65193592:G:A,NC_000017.11:65193592:G:C
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65193593G>A, NC_000017.11:g.65193593G>C, NC_000017.10:g.63189711G>A, NC_000017.10:g.63189711G>C, NG_013021.2:g.61256G>A, NG_013021.2:g.61256G>C, NM_003835.4:c.797G>A, NM_003835.4:c.797G>C, NM_003835.3:c.797G>A, NM_003835.3:c.797G>C, NM_001081955.3:c.788G>A, NM_001081955.3:c.788G>C, NM_001081955.2:c.788G>A, NM_001081955.2:c.788G>C, NM_001165933.2:c.788G>A, NM_001165933.2:c.788G>C, NM_001165933.1:c.788G>A, NM_001165933.1:c.788G>C, NP_003826.2:p.Gly266Asp, NP_003826.2:p.Gly266Ala, NP_001075424.1:p.Gly263Asp, NP_001075424.1:p.Gly263Ala, NP_001159405.1:p.Gly263Asp, NP_001159405.1:p.Gly263Ala

Select item 14857613467.

rs1485761346 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:65160315 (GRCh38)
17:63156433 (GRCh37)
Canonical SPDI:: NC_000017.11:65160314:T:C
Gene:: RGS9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65160315T>C, NC_000017.10:g.63156433T>C, NG_013021.2:g.27978T>C, NM_003835.4:c.288T>C, NM_003835.3:c.288T>C, NM_001081955.3:c.288T>C, NM_001081955.2:c.288T>C, NM_001165933.2:c.288T>C, NM_001165933.1:c.288T>C

Select item 14855094628.

rs1485509462 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65225215 (GRCh38)
17:63221333 (GRCh37)
Canonical SPDI:: NC_000017.11:65225214:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65225215G>A, NC_000017.10:g.63221333G>A, NG_013021.2:g.92878G>A, NM_003835.4:c.1621G>A, NM_003835.3:c.1621G>A, NM_001081955.3:c.1612G>A, NM_001081955.2:c.1612G>A, NP_003826.2:p.Glu541Lys, NP_001075424.1:p.Glu538Lys

Select item 14832131829.

rs1483213182 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65137576 (GRCh38)
17:63133694 (GRCh37)
Canonical SPDI:: NC_000017.11:65137575:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.65137576G>A, NC_000017.10:g.63133694G>A, NG_013021.2:g.5239G>A, NM_003835.4:c.36G>A, NM_003835.3:c.36G>A, NM_001081955.3:c.36G>A, NM_001081955.2:c.36G>A, NM_001165933.2:c.36G>A, NM_001165933.1:c.36G>A

Select item 148109644110.

rs1481096441 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:65225275 (GRCh38)
17:63221393 (GRCh37)
Canonical SPDI:: NC_000017.11:65225274:C:T
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa
MAF:: T=0.00005/1 (ALFA)
HGVS:: NC_000017.11:g.65225275C>T, NC_000017.10:g.63221393C>T, NG_013021.2:g.92938C>T, NM_003835.4:c.1681C>T, NM_003835.3:c.1681C>T, NM_001081955.3:c.1672C>T, NM_001081955.2:c.1672C>T, NP_003826.2:p.Leu561Phe, NP_001075424.1:p.Leu558Phe

Select item 147788707711.

rs1477887077 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:65204260 (GRCh38)
17:63200378 (GRCh37)
Canonical SPDI:: NC_000017.11:65204259:C:G
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65204260C>G, NC_000017.10:g.63200378C>G, NG_013021.2:g.71923C>G, NM_003835.4:c.1162C>G, NM_003835.3:c.1162C>G, NM_001081955.3:c.1153C>G, NM_001081955.2:c.1153C>G, NM_001165933.2:c.1153C>G, NM_001165933.1:c.1153C>G, NP_003826.2:p.Leu388Val, NP_001075424.1:p.Leu385Val, NP_001159405.1:p.Leu385Val

Select item 147668806612.

rs1476688066 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65210579 (GRCh38)
17:63206697 (GRCh37)
Canonical SPDI:: NC_000017.11:65210578:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000012/3 (GnomAD_exomes)
A=0.000023/6 (TOPMED)
HGVS:: NC_000017.11:g.65210579G>A, NC_000017.10:g.63206697G>A, NG_013021.2:g.78242G>A, NM_003835.4:c.1381G>A, NM_003835.3:c.1381G>A, NM_001081955.3:c.1372G>A, NM_001081955.2:c.1372G>A, NM_001165933.2:c.1372G>A, NM_001165933.1:c.1372G>A, NP_003826.2:p.Ala461Thr, NP_001075424.1:p.Ala458Thr, NP_001159405.1:p.Ala458Thr

Select item 147663699913.

rs1476636999 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:65225379 (GRCh38)
17:63221497 (GRCh37)
Canonical SPDI:: NC_000017.11:65225378:C:T
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65225379C>T, NC_000017.10:g.63221497C>T, NG_013021.2:g.93042C>T, NM_003835.4:c.1785C>T, NM_003835.3:c.1785C>T, NM_001081955.3:c.1776C>T, NM_001081955.2:c.1776C>T

Select item 147467407914.

rs1474674079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:65193559 (GRCh38)
17:63189677 (GRCh37)
Canonical SPDI:: NC_000017.11:65193558:G:A,NC_000017.11:65193558:G:C
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00003/1 (ALFA)
HGVS:: NC_000017.11:g.65193559G>A, NC_000017.11:g.65193559G>C, NC_000017.10:g.63189677G>A, NC_000017.10:g.63189677G>C, NG_013021.2:g.61222G>A, NG_013021.2:g.61222G>C, NM_003835.4:c.763G>A, NM_003835.4:c.763G>C, NM_003835.3:c.763G>A, NM_003835.3:c.763G>C, NM_001081955.3:c.754G>A, NM_001081955.3:c.754G>C, NM_001081955.2:c.754G>A, NM_001081955.2:c.754G>C, NM_001165933.2:c.754G>A, NM_001165933.2:c.754G>C, NM_001165933.1:c.754G>A, NM_001165933.1:c.754G>C, NP_003826.2:p.Glu255Lys, NP_003826.2:p.Glu255Gln, NP_001075424.1:p.Glu252Lys, NP_001075424.1:p.Glu252Gln, NP_001159405.1:p.Glu252Lys, NP_001159405.1:p.Glu252Gln

Select item 147340649215.

rs1473406492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65137560 (GRCh38)
17:63133678 (GRCh37)
Canonical SPDI:: NC_000017.11:65137559:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65137560G>A, NC_000017.10:g.63133678G>A, NG_013021.2:g.5223G>A, NM_003835.4:c.20G>A, NM_003835.3:c.20G>A, NM_001081955.3:c.20G>A, NM_001081955.2:c.20G>A, NM_001165933.2:c.20G>A, NM_001165933.1:c.20G>A, NP_003826.2:p.Gly7Asp, NP_001075424.1:p.Gly7Asp, NP_001159405.1:p.Gly7Asp

Select item 147300506616.

rs1473005066 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:65225429 (GRCh38)
17:63221547 (GRCh37)
Canonical SPDI:: NC_000017.11:65225428:A:C
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.65225429A>C, NC_000017.10:g.63221547A>C, NG_013021.2:g.93092A>C, NM_003835.4:c.1835A>C, NM_003835.3:c.1835A>C, NM_001081955.3:c.1826A>C, NM_001081955.2:c.1826A>C, NP_003826.2:p.Gln612Pro, NP_001075424.1:p.Gln609Pro

Select item 147193392017.

rs1471933920 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:65197234 (GRCh38)
17:63193352 (GRCh37)
Canonical SPDI:: NC_000017.11:65197233:A:G
Gene:: RGS9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65197234A>G, NC_000017.10:g.63193352A>G, NG_013021.2:g.64897A>G, NM_003835.4:c.969A>G, NM_003835.3:c.969A>G, NM_001081955.3:c.960A>G, NM_001081955.2:c.960A>G, NM_001165933.2:c.960A>G, NM_001165933.1:c.960A>G

Select item 146841533318.

rs1468415333 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65225038 (GRCh38)
17:63221156 (GRCh37)
Canonical SPDI:: NC_000017.11:65225037:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.65225038G>A, NC_000017.10:g.63221156G>A, NG_013021.2:g.92701G>A, NM_003835.4:c.1444G>A, NM_003835.3:c.1444G>A, NM_001081955.3:c.1435G>A, NM_001081955.2:c.1435G>A, NP_003826.2:p.Val482Met, NP_001075424.1:p.Val479Met

Select item 146765372419.

rs1467653724 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:65197178 (GRCh38)
17:63193296 (GRCh37)
Canonical SPDI:: NC_000017.11:65197177:G:A
Gene:: RGS9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.65197178G>A, NC_000017.10:g.63193296G>A, NG_013021.2:g.64841G>A, NM_003835.4:c.913G>A, NM_003835.3:c.913G>A, NM_001081955.3:c.904G>A, NM_001081955.2:c.904G>A, NM_001165933.2:c.904G>A, NM_001165933.1:c.904G>A, NP_003826.2:p.Glu305Lys, NP_001075424.1:p.Glu302Lys, NP_001159405.1:p.Glu302Lys

Select item 146739200520.

rs1467392005 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:65225179 (GRCh38)
17:63221297 (GRCh37)
Canonical SPDI:: NC_000017.11:65225178:G:T
Gene:: RGS9 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.65225179G>T, NC_000017.10:g.63221297G>T, NG_013021.2:g.92842G>T, NM_003835.4:c.1585G>T, NM_003835.3:c.1585G>T, NM_001081955.3:c.1576G>T, NM_001081955.2:c.1576G>T, NP_003826.2:p.Ala529Ser, NP_001075424.1:p.Ala526Ser

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