SNP Links for Protein (Select 304434798) - SNP

Links from Protein

Items: 1 to 20 of 624

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Select item 14874481411.

rs1487448141 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:13010227 (GRCh38)
11:13031774 (GRCh37)
Canonical SPDI:: NC_000011.10:13010226:C:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.13010227C>A, NC_000011.9:g.13031774C>A, NM_001080521.3:c.651C>A, NM_001080521.2:c.651C>A, NP_001073990.2:p.His217Gln

Select item 14873665132.

rs1487366513 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:13010199 (GRCh38)
11:13031746 (GRCh37)
Canonical SPDI:: NC_000011.10:13010198:C:G
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000005/1 (GnomAD_exomes)
G=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.13010199C>G, NC_000011.9:g.13031746C>G, NM_001080521.3:c.623C>G, NM_001080521.2:c.623C>G, NP_001073990.2:p.Ser208Trp

Select item 14866400573.

rs1486640057 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:13010434 (GRCh38)
11:13031981 (GRCh37)
Canonical SPDI:: NC_000011.10:13010433:C:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,2KB_upstream_variant,upstream_transcript_variant
HGVS:: NC_000011.10:g.13010434C>T, NC_000011.9:g.13031981C>T, NM_001080521.3:c.858C>T, NM_001080521.2:c.858C>T

Select item 14866094904.

rs1486609490 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:13011048 (GRCh38)
11:13032595 (GRCh37)
Canonical SPDI:: NC_000011.10:13011047:C:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13011048C>A, NC_000011.9:g.13032595C>A, NM_001080521.3:c.1472C>A, NM_001080521.2:c.1472C>A, NP_001073990.2:p.Ser491Tyr

Select item 14856527455.

rs1485652745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 11:13010705 (GRCh38)
11:13032252 (GRCh37)
Canonical SPDI:: NC_000011.10:13010704:G:A,NC_000011.10:13010704:G:C,NC_000011.10:13010704:G:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13010705G>A, NC_000011.10:g.13010705G>C, NC_000011.10:g.13010705G>T, NC_000011.9:g.13032252G>A, NC_000011.9:g.13032252G>C, NC_000011.9:g.13032252G>T, NM_001080521.3:c.1129G>A, NM_001080521.3:c.1129G>C, NM_001080521.3:c.1129G>T, NM_001080521.2:c.1129G>A, NM_001080521.2:c.1129G>C, NM_001080521.2:c.1129G>T, NP_001073990.2:p.Gly377Ser, NP_001073990.2:p.Gly377Arg, NP_001073990.2:p.Gly377Cys

Select item 14846733166.

rs1484673316 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:13010968 (GRCh38)
11:13032515 (GRCh37)
Canonical SPDI:: NC_000011.10:13010967:C:A,NC_000011.10:13010967:C:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000031/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.13010968C>A, NC_000011.10:g.13010968C>T, NC_000011.9:g.13032515C>A, NC_000011.9:g.13032515C>T, NM_001080521.3:c.1392C>A, NM_001080521.3:c.1392C>T, NM_001080521.2:c.1392C>A, NM_001080521.2:c.1392C>T

Select item 14843624537.

rs1484362453 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:13009872 (GRCh38)
11:13031419 (GRCh37)
Canonical SPDI:: NC_000011.10:13009871:G:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.13009872G>A, NC_000011.9:g.13031419G>A, NM_001080521.3:c.296G>A, NM_001080521.2:c.296G>A, NP_001073990.2:p.Gly99Asp

Select item 14830796298.

rs1483079629 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:13009582 (GRCh38)
11:13031129 (GRCh37)
Canonical SPDI:: NC_000011.10:13009581:T:C,NC_000011.10:13009581:T:G
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: 2KB_upstream_variant,synonymous_variant,coding_sequence_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
C=0.000008/2 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.13009582T>C, NC_000011.10:g.13009582T>G, NC_000011.9:g.13031129T>C, NC_000011.9:g.13031129T>G, NM_001080521.3:c.6T>C, NM_001080521.3:c.6T>G, NM_001080521.2:c.6T>C, NM_001080521.2:c.6T>G, NP_001073990.2:p.Asp2Glu

Select item 14828938389.

rs1482893838 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCCCGGCGCTGCGACGACTTGCTG>- [Show Flanks]
Chromosome:: 11:13010543 (GRCh38)
11:13032090 (GRCh37)
Canonical SPDI:: NC_000011.10:13010538:GCTGGCCCGGCGCTGCGACGACTTGCTG:GCTG
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: inframe_deletion,upstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GCTG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.13010543_13010566del, NC_000011.9:g.13032090_13032113del, NM_001080521.3:c.967_990del, NM_001080521.2:c.967_990del, NP_001073990.2:p.Ala323_Leu330del

Select item 148137051510.

rs1481370515 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:13009628 (GRCh38)
11:13031175 (GRCh37)
Canonical SPDI:: NC_000011.10:13009627:C:G,NC_000011.10:13009627:C:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: 2KB_upstream_variant,synonymous_variant,coding_sequence_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.13009628C>G, NC_000011.10:g.13009628C>T, NC_000011.9:g.13031175C>G, NC_000011.9:g.13031175C>T, NM_001080521.3:c.52C>G, NM_001080521.3:c.52C>T, NM_001080521.2:c.52C>G, NM_001080521.2:c.52C>T, NP_001073990.2:p.Leu18Val

Select item 147758771111.

rs1477587711 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:13009881 (GRCh38)
11:13031428 (GRCh37)
Canonical SPDI:: NC_000011.10:13009880:G:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13009881G>T, NC_000011.9:g.13031428G>T, NM_001080521.3:c.305G>T, NM_001080521.2:c.305G>T, NP_001073990.2:p.Arg102Leu

Select item 147705229912.

rs1477052299 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:13010712 (GRCh38)
11:13032259 (GRCh37)
Canonical SPDI:: NC_000011.10:13010711:C:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant
HGVS:: NC_000011.10:g.13010712C>A, NC_000011.9:g.13032259C>A, NM_001080521.3:c.1136C>A, NM_001080521.2:c.1136C>A, NP_001073990.2:p.Pro379His

Select item 147694753513.

rs1476947535 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:13010048 (GRCh38)
11:13031595 (GRCh37)
Canonical SPDI:: NC_000011.10:13010047:C:G,NC_000011.10:13010047:C:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000057/2 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.13010048C>G, NC_000011.10:g.13010048C>T, NC_000011.9:g.13031595C>G, NC_000011.9:g.13031595C>T, NM_001080521.3:c.472C>G, NM_001080521.3:c.472C>T, NM_001080521.2:c.472C>G, NM_001080521.2:c.472C>T, NP_001073990.2:p.Arg158Gly, NP_001073990.2:p.Arg158Cys

Select item 147516627914.

rs1475166279 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:13010658 (GRCh38)
11:13032205 (GRCh37)
Canonical SPDI:: NC_000011.10:13010657:G:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.13010658G>A, NC_000011.9:g.13032205G>A, NM_001080521.3:c.1082G>A, NM_001080521.2:c.1082G>A, NP_001073990.2:p.Arg361Gln

Select item 147351376015.

rs1473513760 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:13009821 (GRCh38)
11:13031368 (GRCh37)
Canonical SPDI:: NC_000011.10:13009820:G:A,NC_000011.10:13009820:G:C
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
A=0.000013/3 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13009821G>A, NC_000011.10:g.13009821G>C, NC_000011.9:g.13031368G>A, NC_000011.9:g.13031368G>C, NM_001080521.3:c.245G>A, NM_001080521.3:c.245G>C, NM_001080521.2:c.245G>A, NM_001080521.2:c.245G>C, NP_001073990.2:p.Gly82Asp, NP_001073990.2:p.Gly82Ala

Select item 147156635916.

rs1471566359 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:13009780 (GRCh38)
11:13031327 (GRCh37)
Canonical SPDI:: NC_000011.10:13009779:G:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: upstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13009780G>T, NC_000011.9:g.13031327G>T, NM_001080521.3:c.204G>T, NM_001080521.2:c.204G>T

Select item 147153607917.

rs1471536079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:13010332 (GRCh38)
11:13031879 (GRCh37)
Canonical SPDI:: NC_000011.10:13010331:G:A,NC_000011.10:13010331:G:C
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: 2KB_upstream_variant,synonymous_variant,coding_sequence_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000214/3 (ALFA)
C=0.000013/2 (GnomAD_exomes)
C=0.000036/5 (GnomAD)
C=0.000045/12 (TOPMED)
A=0.000343/1 (KOREAN)
HGVS:: NC_000011.10:g.13010332G>A, NC_000011.10:g.13010332G>C, NC_000011.9:g.13031879G>A, NC_000011.9:g.13031879G>C, NM_001080521.3:c.756G>A, NM_001080521.3:c.756G>C, NM_001080521.2:c.756G>A, NM_001080521.2:c.756G>C, NP_001073990.2:p.Glu252Asp

Select item 146868506118.

rs1468685061 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:13010896 (GRCh38)
11:13032443 (GRCh37)
Canonical SPDI:: NC_000011.10:13010895:G:A
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.13010896G>A, NC_000011.9:g.13032443G>A, NM_001080521.3:c.1320G>A, NM_001080521.2:c.1320G>A

Select item 146758483719.

rs1467584837 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:13009602 (GRCh38)
11:13031149 (GRCh37)
Canonical SPDI:: NC_000011.10:13009601:C:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000017/4 (GnomAD_exomes)
T=0.000343/1 (KOREAN)
HGVS:: NC_000011.10:g.13009602C>T, NC_000011.9:g.13031149C>T, NM_001080521.3:c.26C>T, NM_001080521.2:c.26C>T, NP_001073990.2:p.Ser9Leu

Select item 146627763620.

rs1466277636 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:13009623 (GRCh38)
11:13031170 (GRCh37)
Canonical SPDI:: NC_000011.10:13009622:A:G,NC_000011.10:13009622:A:T
Gene:: RASSF10 (Varview), RASSF10-DT (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.13009623A>G, NC_000011.10:g.13009623A>T, NC_000011.9:g.13031170A>G, NC_000011.9:g.13031170A>T, NM_001080521.3:c.47A>G, NM_001080521.3:c.47A>T, NM_001080521.2:c.47A>G, NM_001080521.2:c.47A>T, NP_001073990.2:p.Glu16Gly, NP_001073990.2:p.Glu16Val

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