SNP Links for Protein (Select 530403303) - SNP

Links from Protein

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Select item 14900554211.

rs1490055421 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:59355309 (GRCh38)
14:59822027 (GRCh37)
Canonical SPDI:: NC_000014.9:59355308:C:T
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59355309C>T, NC_000014.8:g.59822027C>T, NG_047127.1:g.171699C>T, NM_001270520.2:c.2501C>T, NM_001270520.1:c.2501C>T, NM_014992.2:c.2531C>T, XM_005267430.3:c.2531C>T, XM_005267430.2:c.2531C>T, XM_005267430.1:c.2531C>T, XM_005267431.2:c.2531C>T, XM_005267431.1:c.2531C>T, XM_047431135.1:c.2501C>T, NP_001257449.1:p.Ala834Val, NP_055807.1:p.Ala844Val, XP_005267487.1:p.Ala844Val, XP_005267488.1:p.Ala844Val, XP_047287091.1:p.Ala834Val

Select item 14885512872.

rs1488551287 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:59359459 (GRCh38)
14:59826177 (GRCh37)
Canonical SPDI:: NC_000014.9:59359458:A:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000014.9:g.59359459A>G, NC_000014.8:g.59826177A>G, NG_047127.1:g.175849A>G, NM_001270520.2:c.2588A>G, NM_001270520.1:c.2588A>G, NM_014992.2:c.2618A>G, XM_005267430.3:c.2618A>G, XM_005267430.2:c.2618A>G, XM_005267430.1:c.2618A>G, XM_005267431.2:c.2618A>G, XM_005267431.1:c.2618A>G, XM_047431135.1:c.2588A>G, NP_001257449.1:p.Asn863Ser, NP_055807.1:p.Asn873Ser, XP_005267487.1:p.Asn873Ser, XP_005267488.1:p.Asn873Ser, XP_047287091.1:p.Asn863Ser

Select item 14884383723.

rs1488438372 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:59340087 (GRCh38)
14:59806805 (GRCh37)
Canonical SPDI:: NC_000014.9:59340086:C:A
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000014.9:g.59340087C>A, NC_000014.8:g.59806805C>A, NG_047127.1:g.156477C>A, NM_001270520.2:c.1982C>A, NM_001270520.1:c.1982C>A, NM_014992.2:c.2012C>A, XM_005267430.3:c.2012C>A, XM_005267430.2:c.2012C>A, XM_005267430.1:c.2012C>A, XM_005267431.2:c.2012C>A, XM_005267431.1:c.2012C>A, XM_047431135.1:c.1982C>A, NP_001257449.1:p.Ala661Asp, NP_055807.1:p.Ala671Asp, XP_005267487.1:p.Ala671Asp, XP_005267488.1:p.Ala671Asp, XP_047287091.1:p.Ala661Asp

Select item 14871878454.

rs1487187845 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 14:59330673 (GRCh38)
14:59797391 (GRCh37)
Canonical SPDI:: NC_000014.9:59330672:C:A,NC_000014.9:59330672:C:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000014.9:g.59330673C>A, NC_000014.9:g.59330673C>G, NC_000014.8:g.59797391C>A, NC_000014.8:g.59797391C>G, NG_047127.1:g.147063C>A, NG_047127.1:g.147063C>G, NM_001270520.2:c.1545C>A, NM_001270520.2:c.1545C>G, NM_001270520.1:c.1545C>A, NM_001270520.1:c.1545C>G, NM_014992.2:c.1545C>A, NM_014992.2:c.1545C>G, XM_005267430.3:c.1545C>A, XM_005267430.3:c.1545C>G, XM_005267430.2:c.1545C>A, XM_005267430.2:c.1545C>G, XM_005267430.1:c.1545C>A, XM_005267430.1:c.1545C>G, XM_005267431.2:c.1545C>A, XM_005267431.2:c.1545C>G, XM_005267431.1:c.1545C>A, XM_005267431.1:c.1545C>G, XM_047431135.1:c.1545C>A, XM_047431135.1:c.1545C>G

Select item 14866383135.

rs1486638313 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:59347583 (GRCh38)
14:59814301 (GRCh37)
Canonical SPDI:: NC_000014.9:59347582:T:C
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59347583T>C, NC_000014.8:g.59814301T>C, NG_047127.1:g.163973T>C, NM_001270520.2:c.2120T>C, NM_001270520.1:c.2120T>C, NM_014992.2:c.2150T>C, XM_005267430.3:c.2150T>C, XM_005267430.2:c.2150T>C, XM_005267430.1:c.2150T>C, XM_005267431.2:c.2150T>C, XM_005267431.1:c.2150T>C, XM_047431135.1:c.2120T>C, NP_001257449.1:p.Met707Thr, NP_055807.1:p.Met717Thr, XP_005267487.1:p.Met717Thr, XP_005267488.1:p.Met717Thr, XP_047287091.1:p.Met707Thr

Select item 14859727616.

rs1485972761 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:59322908 (GRCh38)
14:59789626 (GRCh37)
Canonical SPDI:: NC_000014.9:59322907:A:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59322908A>G, NC_000014.8:g.59789626A>G, NG_047127.1:g.139298A>G, NM_001270520.2:c.457A>G, NM_001270520.1:c.457A>G, NM_014992.2:c.457A>G, XM_005267430.3:c.457A>G, XM_005267430.2:c.457A>G, XM_005267430.1:c.457A>G, XM_005267431.2:c.457A>G, XM_005267431.1:c.457A>G, XM_047431135.1:c.457A>G, NP_001257449.1:p.Ile153Val, NP_055807.1:p.Ile153Val, XP_005267487.1:p.Ile153Val, XP_005267488.1:p.Ile153Val, XP_047287091.1:p.Ile153Val

Select item 14855178477.

rs1485517847 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:59320566 (GRCh38)
14:59787284 (GRCh37)
Canonical SPDI:: NC_000014.9:59320565:T:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.59320566T>G, NC_000014.8:g.59787284T>G, NG_047127.1:g.136956T>G, NM_001270520.2:c.422T>G, NM_001270520.1:c.422T>G, NM_014992.2:c.422T>G, XM_005267430.3:c.422T>G, XM_005267430.2:c.422T>G, XM_005267430.1:c.422T>G, XM_005267431.2:c.422T>G, XM_005267431.1:c.422T>G, XM_047431135.1:c.422T>G, NP_001257449.1:p.Leu141Arg, NP_055807.1:p.Leu141Arg, XP_005267487.1:p.Leu141Arg, XP_005267488.1:p.Leu141Arg, XP_047287091.1:p.Leu141Arg

Select item 14853175608.

rs1485317560 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:59324445 (GRCh38)
14:59791163 (GRCh37)
Canonical SPDI:: NC_000014.9:59324444:C:T
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000026/7 (TOPMED)
T=0.00005/7 (GnomAD)
HGVS:: NC_000014.9:g.59324445C>T, NC_000014.8:g.59791163C>T, NG_047127.1:g.140835C>T, NM_001270520.2:c.980C>T, NM_001270520.1:c.980C>T, NM_014992.2:c.980C>T, XM_005267430.3:c.980C>T, XM_005267430.2:c.980C>T, XM_005267430.1:c.980C>T, XM_005267431.2:c.980C>T, XM_005267431.1:c.980C>T, XM_047431135.1:c.980C>T, NP_001257449.1:p.Thr327Ile, NP_055807.1:p.Thr327Ile, XP_005267487.1:p.Thr327Ile, XP_005267488.1:p.Thr327Ile, XP_047287091.1:p.Thr327Ile

Select item 14845352369.

rs1484535236 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:59352594 (GRCh38)
14:59819312 (GRCh37)
Canonical SPDI:: NC_000014.9:59352593:G:A
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.59352594G>A, NC_000014.8:g.59819312G>A, NG_047127.1:g.168984G>A, NM_001270520.2:c.2229G>A, NM_001270520.1:c.2229G>A, NM_014992.2:c.2259G>A, XM_005267430.3:c.2259G>A, XM_005267430.2:c.2259G>A, XM_005267430.1:c.2259G>A, XM_005267431.2:c.2259G>A, XM_005267431.1:c.2259G>A, XM_047431135.1:c.2229G>A

Select item 148350087510.

rs1483500875 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:59368718 (GRCh38)
14:59835436 (GRCh37)
Canonical SPDI:: NC_000014.9:59368717:G:A
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59368718G>A, NC_000014.8:g.59835436G>A, NG_047127.1:g.185108G>A, NM_001270520.2:c.3066G>A, NM_001270520.1:c.3066G>A, NM_014992.2:c.3096G>A, XM_005267430.3:c.3096G>A, XM_005267430.2:c.3096G>A, XM_005267430.1:c.3096G>A, XM_005267431.2:c.3096G>A, XM_005267431.1:c.3096G>A, XM_047431135.1:c.3066G>A

Select item 148274336911.

rs1482743369 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:59263570 (GRCh38)
14:59730288 (GRCh37)
Canonical SPDI:: NC_000014.9:59263569:A:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: G=0.0022/4 (Korea1K)
HGVS:: NC_000014.9:g.59263570A>G, NC_000014.8:g.59730288A>G, NG_047127.1:g.79960A>G, NM_001270520.2:c.93A>G, NM_001270520.1:c.93A>G, NM_014992.2:c.93A>G, XM_005267430.3:c.93A>G, XM_005267430.2:c.93A>G, XM_005267430.1:c.93A>G, XM_005267431.2:c.93A>G, XM_005267431.1:c.93A>G, XM_047431135.1:c.93A>G

Select item 148216135912.

rs1482161359 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:59322933 (GRCh38)
14:59789651 (GRCh37)
Canonical SPDI:: NC_000014.9:59322932:T:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.59322933T>G, NC_000014.8:g.59789651T>G, NG_047127.1:g.139323T>G, NM_001270520.2:c.482T>G, NM_001270520.1:c.482T>G, NM_014992.2:c.482T>G, XM_005267430.3:c.482T>G, XM_005267430.2:c.482T>G, XM_005267430.1:c.482T>G, XM_005267431.2:c.482T>G, XM_005267431.1:c.482T>G, XM_047431135.1:c.482T>G, NP_001257449.1:p.Ile161Ser, NP_055807.1:p.Ile161Ser, XP_005267487.1:p.Ile161Ser, XP_005267488.1:p.Ile161Ser, XP_047287091.1:p.Ile161Ser

Select item 148164363813.

rs1481643638 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:59322985 (GRCh38)
14:59789703 (GRCh37)
Canonical SPDI:: NC_000014.9:59322984:T:C
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: C=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59322985T>C, NC_000014.8:g.59789703T>C, NG_047127.1:g.139375T>C, NM_001270520.2:c.534T>C, NM_001270520.1:c.534T>C, NM_014992.2:c.534T>C, XM_005267430.3:c.534T>C, XM_005267430.2:c.534T>C, XM_005267430.1:c.534T>C, XM_005267431.2:c.534T>C, XM_005267431.1:c.534T>C, XM_047431135.1:c.534T>C

Select item 148102608214.

rs1481026082 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:59360802 (GRCh38)
14:59827520 (GRCh37)
Canonical SPDI:: NC_000014.9:59360801:C:T
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59360802C>T, NC_000014.8:g.59827520C>T, NG_047127.1:g.177192C>T, NM_001270520.2:c.2634C>T, NM_001270520.1:c.2634C>T, NM_014992.2:c.2664C>T, XM_005267430.3:c.2664C>T, XM_005267430.2:c.2664C>T, XM_005267430.1:c.2664C>T, XM_005267431.2:c.2664C>T, XM_005267431.1:c.2664C>T, XM_047431135.1:c.2634C>T

Select item 147989852615.

rs1479898526 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:59355220 (GRCh38)
14:59821938 (GRCh37)
Canonical SPDI:: NC_000014.9:59355219:G:A
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59355220G>A, NC_000014.8:g.59821938G>A, NG_047127.1:g.171610G>A, NM_001270520.2:c.2412G>A, NM_001270520.1:c.2412G>A, NM_014992.2:c.2442G>A, XM_005267430.3:c.2442G>A, XM_005267430.2:c.2442G>A, XM_005267430.1:c.2442G>A, XM_005267431.2:c.2442G>A, XM_005267431.1:c.2442G>A, XM_047431135.1:c.2412G>A

Select item 147922953616.

rs1479229536 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:59368756 (GRCh38)
14:59835474 (GRCh37)
Canonical SPDI:: NC_000014.9:59368755:T:C
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.59368756T>C, NC_000014.8:g.59835474T>C, NG_047127.1:g.185146T>C, NM_001270520.2:c.3104T>C, NM_001270520.1:c.3104T>C, NM_014992.2:c.3134T>C, XM_005267430.3:c.3134T>C, XM_005267430.2:c.3134T>C, XM_005267430.1:c.3134T>C, XM_005267431.2:c.3134T>C, XM_005267431.1:c.3134T>C, XM_047431135.1:c.3104T>C, NP_001257449.1:p.Val1035Ala, NP_055807.1:p.Val1045Ala, XP_005267487.1:p.Val1045Ala, XP_005267488.1:p.Val1045Ala, XP_047287091.1:p.Val1035Ala

Select item 147854458317.

rs1478544583 [Homo sapiens]

Variant type:: DEL
Alleles:: AGGTGGGATGCTT>- [Show Flanks]
Chromosome:: 14:59331322 (GRCh38)
14:59798040 (GRCh37)
Canonical SPDI:: NC_000014.9:59331321:AGGTGGGATGCTT:
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000014.9:g.59331322_59331334del, NC_000014.8:g.59798040_59798052del, NG_047127.1:g.147712_147724del, NM_001270520.2:c.1674_1686del, NM_001270520.1:c.1674_1686del, NM_014992.2:c.1674_1686del, XM_005267430.3:c.1674_1686del, XM_005267430.2:c.1674_1686del, XM_005267430.1:c.1674_1686del, XM_005267431.2:c.1674_1686del, XM_005267431.1:c.1674_1686del, XM_047431135.1:c.1674_1686del, NP_001257449.1:p.Gly559fs, NP_055807.1:p.Gly559fs, XP_005267487.1:p.Gly559fs, XP_005267488.1:p.Gly559fs, XP_047287091.1:p.Gly559fs

Select item 147820365118.

rs1478203651 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:59360824 (GRCh38)
14:59827542 (GRCh37)
Canonical SPDI:: NC_000014.9:59360823:A:G
Gene:: DAAM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.59360824A>G, NC_000014.8:g.59827542A>G, NG_047127.1:g.177214A>G, NM_001270520.2:c.2656A>G, NM_001270520.1:c.2656A>G, NM_014992.2:c.2686A>G, XM_005267430.3:c.2686A>G, XM_005267430.2:c.2686A>G, XM_005267430.1:c.2686A>G, XM_005267431.2:c.2686A>G, XM_005267431.1:c.2686A>G, XM_047431135.1:c.2656A>G, NP_001257449.1:p.Ile886Val, NP_055807.1:p.Ile896Val, XP_005267487.1:p.Ile896Val, XP_005267488.1:p.Ile896Val, XP_047287091.1:p.Ile886Val

Select item 147656433719.

rs1476564337 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:59326960 (GRCh38)
14:59793678 (GRCh37)
Canonical SPDI:: NC_000014.9:59326959:G:T
Gene:: DAAM1 (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=0.000029/4 (GnomAD)
HGVS:: NC_000014.9:g.59326960G>T, NC_000014.8:g.59793678G>T, NG_047127.1:g.143350G>T, NM_001270520.2:c.1341G>T, NM_001270520.1:c.1341G>T, NM_014992.2:c.1341G>T, XM_005267430.3:c.1341G>T, XM_005267430.2:c.1341G>T, XM_005267430.1:c.1341G>T, XM_005267431.2:c.1341G>T, XM_005267431.1:c.1341G>T, XM_047431135.1:c.1341G>T, NP_001257449.1:p.Gln447His, NP_055807.1:p.Gln447His, XP_005267487.1:p.Gln447His, XP_005267488.1:p.Gln447His, XP_047287091.1:p.Gln447His

Select item 147618766320.

rs1476187663 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:59353913 (GRCh38)
14:59820631 (GRCh37)
Canonical SPDI:: NC_000014.9:59353912:T:A
Gene:: DAAM1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.59353913T>A, NC_000014.8:g.59820631T>A, NG_047127.1:g.170303T>A, NM_001270520.2:c.2305T>A, NM_001270520.1:c.2305T>A, NM_014992.2:c.2335T>A, XM_005267430.3:c.2335T>A, XM_005267430.2:c.2335T>A, XM_005267430.1:c.2335T>A, XM_005267431.2:c.2335T>A, XM_005267431.1:c.2335T>A, XM_047431135.1:c.2305T>A, NP_001257449.1:p.Phe769Ile, NP_055807.1:p.Phe779Ile, XP_005267487.1:p.Phe779Ile, XP_005267488.1:p.Phe779Ile, XP_047287091.1:p.Phe769Ile

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