SNP Links for Protein (Select 767931301) - SNP

Links from Protein

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Select item 14897913621.

rs1489791362 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:87662274 (GRCh38)
4:88583426 (GRCh37)
Canonical SPDI:: NC_000004.12:87662273:A:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87662274A>C, NC_000004.11:g.88583426A>C, NG_008988.1:g.16973A>C, NM_004407.4:c.496A>C, NM_004407.3:c.496A>C, NM_001079911.3:c.448A>C, NM_001079911.2:c.448A>C, XM_011531705.3:c.583A>C, XM_011531705.2:c.583A>C, XM_011531705.1:c.583A>C, XM_011531706.3:c.535A>C, XM_011531706.2:c.535A>C, XM_011531706.1:c.535A>C

Select item 14885880402.

rs1488588040 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:87663318 (GRCh38)
4:88584470 (GRCh37)
Canonical SPDI:: NC_000004.12:87663317:T:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,stop_lost,terminator_codon_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_000004.12:g.87663318T>C, NC_000004.11:g.88584470T>C, NG_008988.1:g.18017T>C, NM_004407.4:c.1540T>C, NM_004407.3:c.1540T>C, NM_001079911.3:c.1492T>C, NM_001079911.2:c.1492T>C, XM_011531705.3:c.1627T>C, XM_011531705.2:c.1627T>C, XM_011531705.1:c.1627T>C, XM_011531706.3:c.1579T>C, XM_011531706.2:c.1579T>C, XM_011531706.1:c.1579T>C, NP_004398.1:p.Ter514Gln, NP_001073380.1:p.Ter498Gln, XP_011530007.1:p.Ter543Gln, XP_011530008.1:p.Ter527Gln

Select item 14884051563.

rs1488405156 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:87657054 (GRCh38)
4:88578206 (GRCh37)
Canonical SPDI:: NC_000004.12:87657053:A:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,500B_downstream_variant,coding_sequence_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87657054A>G, NC_000004.11:g.88578206A>G, NG_008988.1:g.11753A>G, NM_004407.4:c.77A>G, NM_004407.3:c.77A>G, NM_001079911.3:c.77A>G, NM_001079911.2:c.77A>G, XM_011531705.3:c.164A>G, XM_011531705.2:c.164A>G, XM_011531705.1:c.164A>G, XM_011531706.3:c.164A>G, XM_011531706.2:c.164A>G, XM_011531706.1:c.164A>G, NP_004398.1:p.Glu26Gly, NP_001073380.1:p.Glu26Gly, XP_011530007.1:p.Glu55Gly, XP_011530008.1:p.Glu55Gly

Select item 14854580094.

rs1485458009 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:87659248 (GRCh38)
4:88580400 (GRCh37)
Canonical SPDI:: NC_000004.12:87659247:C:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.87659248C>G, NC_000004.11:g.88580400C>G, NG_008988.1:g.13947C>G, NM_004407.4:c.131C>G, NM_004407.3:c.131C>G, NM_001079911.3:c.131C>G, NM_001079911.2:c.131C>G, XM_011531705.3:c.218C>G, XM_011531705.2:c.218C>G, XM_011531705.1:c.218C>G, XM_011531706.3:c.218C>G, XM_011531706.2:c.218C>G, XM_011531706.1:c.218C>G, NP_004398.1:p.Pro44Arg, NP_001073380.1:p.Pro44Arg, XP_011530007.1:p.Pro73Arg, XP_011530008.1:p.Pro73Arg

Select item 14820307245.

rs1482030724 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:87662579 (GRCh38)
4:88583731 (GRCh37)
Canonical SPDI:: NC_000004.12:87662578:T:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87662579T>G, NC_000004.11:g.88583731T>G, NG_008988.1:g.17278T>G, NM_004407.4:c.801T>G, NM_004407.3:c.801T>G, NM_001079911.3:c.753T>G, NM_001079911.2:c.753T>G, XM_011531705.3:c.888T>G, XM_011531705.2:c.888T>G, XM_011531705.1:c.888T>G, XM_011531706.3:c.840T>G, XM_011531706.2:c.840T>G, XM_011531706.1:c.840T>G, NP_004398.1:p.Ile267Met, NP_001073380.1:p.Ile251Met, XP_011530007.1:p.Ile296Met, XP_011530008.1:p.Ile280Met

Select item 14814641146.

rs1481464114 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:87662247 (GRCh38)
4:88583399 (GRCh37)
Canonical SPDI:: NC_000004.12:87662246:A:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.87662247A>G, NC_000004.11:g.88583399A>G, NG_008988.1:g.16946A>G, NM_004407.4:c.469A>G, NM_004407.3:c.469A>G, NM_001079911.3:c.421A>G, NM_001079911.2:c.421A>G, XM_011531705.3:c.556A>G, XM_011531705.2:c.556A>G, XM_011531705.1:c.556A>G, XM_011531706.3:c.508A>G, XM_011531706.2:c.508A>G, XM_011531706.1:c.508A>G, NP_004398.1:p.Ser157Gly, NP_001073380.1:p.Ser141Gly, XP_011530007.1:p.Ser186Gly, XP_011530008.1:p.Ser170Gly

Select item 14810414557.

rs1481041455 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:87663135 (GRCh38)
4:88584287 (GRCh37)
Canonical SPDI:: NC_000004.12:87663134:G:A
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87663135G>A, NC_000004.11:g.88584287G>A, NG_008988.1:g.17834G>A, NM_004407.4:c.1357G>A, NM_004407.3:c.1357G>A, NM_001079911.3:c.1309G>A, NM_001079911.2:c.1309G>A, XM_011531705.3:c.1444G>A, XM_011531705.2:c.1444G>A, XM_011531705.1:c.1444G>A, XM_011531706.3:c.1396G>A, XM_011531706.2:c.1396G>A, XM_011531706.1:c.1396G>A, NP_004398.1:p.Asp453Asn, NP_001073380.1:p.Asp437Asn, XP_011530007.1:p.Asp482Asn, XP_011530008.1:p.Asp466Asn

Select item 14780071948.

rs1478007194 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 4:87663228 (GRCh38)
4:88584380 (GRCh37)
Canonical SPDI:: NC_000004.12:87663227:A:G,NC_000004.12:87663227:A:T
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.87663228A>G, NC_000004.12:g.87663228A>T, NC_000004.11:g.88584380A>G, NC_000004.11:g.88584380A>T, NG_008988.1:g.17927A>G, NG_008988.1:g.17927A>T, NM_004407.4:c.1450A>G, NM_004407.4:c.1450A>T, NM_004407.3:c.1450A>G, NM_004407.3:c.1450A>T, NM_001079911.3:c.1402A>G, NM_001079911.3:c.1402A>T, NM_001079911.2:c.1402A>G, NM_001079911.2:c.1402A>T, XM_011531705.3:c.1537A>G, XM_011531705.3:c.1537A>T, XM_011531705.2:c.1537A>G, XM_011531705.2:c.1537A>T, XM_011531705.1:c.1537A>G, XM_011531705.1:c.1537A>T, XM_011531706.3:c.1489A>G, XM_011531706.3:c.1489A>T, XM_011531706.2:c.1489A>G, XM_011531706.2:c.1489A>T, XM_011531706.1:c.1489A>G, XM_011531706.1:c.1489A>T, NP_004398.1:p.Ile484Val, NP_004398.1:p.Ile484Phe, NP_001073380.1:p.Ile468Val, NP_001073380.1:p.Ile468Phe, XP_011530007.1:p.Ile513Val, XP_011530007.1:p.Ile513Phe, XP_011530008.1:p.Ile497Val, XP_011530008.1:p.Ile497Phe

Select item 14779713409.

rs1477971340 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:87663257 (GRCh38)
4:88584409 (GRCh37)
Canonical SPDI:: NC_000004.12:87663256:T:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87663257T>C, NC_000004.11:g.88584409T>C, NG_008988.1:g.17956T>C, NM_004407.4:c.1479T>C, NM_004407.3:c.1479T>C, NM_001079911.3:c.1431T>C, NM_001079911.2:c.1431T>C, XM_011531705.3:c.1566T>C, XM_011531705.2:c.1566T>C, XM_011531705.1:c.1566T>C, XM_011531706.3:c.1518T>C, XM_011531706.2:c.1518T>C, XM_011531706.1:c.1518T>C

Select item 147789519410.

rs1477895194 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:87662851 (GRCh38)
4:88584003 (GRCh37)
Canonical SPDI:: NC_000004.12:87662850:A:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
G=0.000016/4 (GnomAD_exomes)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000004.12:g.87662851A>G, NC_000004.11:g.88584003A>G, NG_008988.1:g.17550A>G, NM_004407.4:c.1073A>G, NM_004407.3:c.1073A>G, NM_001079911.3:c.1025A>G, NM_001079911.2:c.1025A>G, XM_011531705.3:c.1160A>G, XM_011531705.2:c.1160A>G, XM_011531705.1:c.1160A>G, XM_011531706.3:c.1112A>G, XM_011531706.2:c.1112A>G, XM_011531706.1:c.1112A>G, NP_004398.1:p.Glu358Gly, NP_001073380.1:p.Glu342Gly, XP_011530007.1:p.Glu387Gly, XP_011530008.1:p.Glu371Gly

Select item 147746981111.

rs1477469811 [Homo sapiens]

Variant type:: DEL
Alleles:: AGGTGG>- [Show Flanks]
Chromosome:: 4:87662540 (GRCh38)
4:88583692 (GRCh37)
Canonical SPDI:: NC_000004.12:87662539:AGGTGG:
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: intron_variant,inframe_deletion,coding_sequence_variant
HGVS:: NC_000004.12:g.87662540_87662545del, NC_000004.11:g.88583692_88583697del, NG_008988.1:g.17239_17244del, NM_004407.4:c.762_767del, NM_004407.3:c.762_767del, NM_001079911.3:c.714_719del, NM_001079911.2:c.714_719del, XM_011531705.3:c.849_854del, XM_011531705.2:c.849_854del, XM_011531705.1:c.849_854del, XM_011531706.3:c.801_806del, XM_011531706.2:c.801_806del, XM_011531706.1:c.801_806del, NP_004398.1:p.Gly255_Gly256del, NP_001073380.1:p.Gly239_Gly240del, XP_011530007.1:p.Gly284_Gly285del, XP_011530008.1:p.Gly268_Gly269del

Select item 147587869012.

rs1475878690 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:87657049 (GRCh38)
4:88578201 (GRCh37)
Canonical SPDI:: NC_000004.12:87657048:T:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: coding_sequence_variant,500B_downstream_variant,synonymous_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.87657049T>C, NC_000004.11:g.88578201T>C, NG_008988.1:g.11748T>C, NM_004407.4:c.72T>C, NM_004407.3:c.72T>C, NM_001079911.3:c.72T>C, NM_001079911.2:c.72T>C, XM_011531705.3:c.159T>C, XM_011531705.2:c.159T>C, XM_011531705.1:c.159T>C, XM_011531706.3:c.159T>C, XM_011531706.2:c.159T>C, XM_011531706.1:c.159T>C

Select item 147456844213.

rs1474568442 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:87662596 (GRCh38)
4:88583748 (GRCh37)
Canonical SPDI:: NC_000004.12:87662595:T:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000071/1 (TOMMO)
C=0.000342/1 (KOREAN)
C=0.000546/1 (Korea1K)
HGVS:: NC_000004.12:g.87662596T>C, NC_000004.11:g.88583748T>C, NG_008988.1:g.17295T>C, NM_004407.4:c.818T>C, NM_004407.3:c.818T>C, NM_001079911.3:c.770T>C, NM_001079911.2:c.770T>C, XM_011531705.3:c.905T>C, XM_011531705.2:c.905T>C, XM_011531705.1:c.905T>C, XM_011531706.3:c.857T>C, XM_011531706.2:c.857T>C, XM_011531706.1:c.857T>C, NP_004398.1:p.Ile273Thr, NP_001073380.1:p.Ile257Thr, XP_011530007.1:p.Ile302Thr, XP_011530008.1:p.Ile286Thr

Select item 147400250914.

rs1474002509 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:87659453 (GRCh38)
4:88580605 (GRCh37)
Canonical SPDI:: NC_000004.12:87659452:G:A,NC_000004.12:87659452:G:T
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.87659453G>A, NC_000004.12:g.87659453G>T, NC_000004.11:g.88580605G>A, NC_000004.11:g.88580605G>T, NG_008988.1:g.14152G>A, NG_008988.1:g.14152G>T, NM_004407.4:c.158G>A, NM_004407.4:c.158G>T, NM_004407.3:c.158G>A, NM_004407.3:c.158G>T, XM_011531705.3:c.245G>A, XM_011531705.3:c.245G>T, XM_011531705.2:c.245G>A, XM_011531705.2:c.245G>T, XM_011531705.1:c.245G>A, XM_011531705.1:c.245G>T, NP_004398.1:p.Gly53Asp, NP_004398.1:p.Gly53Val, XP_011530007.1:p.Gly82Asp, XP_011530007.1:p.Gly82Val

Select item 147173083415.

rs1471730834 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACA>- [Show Flanks]
Chromosome:: 4:87662635 (GRCh38)
4:88583787 (GRCh37)
Canonical SPDI:: NC_000004.12:87662628:ACAACAACA:ACAACA
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,inframe_deletion
Validated:: by frequency,by alfa
MAF:: ACAACA=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.87662629ACA[2], NC_000004.11:g.88583781ACA[2], NG_008988.1:g.17328ACA[2], NM_004407.4:c.851ACA[2], NM_004407.3:c.851ACA[2], NM_001079911.3:c.803ACA[2], NM_001079911.2:c.803ACA[2], XM_011531705.3:c.938ACA[2], XM_011531705.2:c.938ACA[2], XM_011531705.1:c.938ACA[2], XM_011531706.3:c.890ACA[2], XM_011531706.2:c.890ACA[2], XM_011531706.1:c.890ACA[2], NP_004398.1:p.Asn286del, NP_001073380.1:p.Asn270del, XP_011530007.1:p.Asn315del, XP_011530008.1:p.Asn299del

Select item 147157741216.

rs1471577412 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:87662307 (GRCh38)
4:88583459 (GRCh37)
Canonical SPDI:: NC_000004.12:87662306:A:C
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.87662307A>C, NC_000004.11:g.88583459A>C, NG_008988.1:g.17006A>C, NM_004407.4:c.529A>C, NM_004407.3:c.529A>C, NM_001079911.3:c.481A>C, NM_001079911.2:c.481A>C, XM_011531705.3:c.616A>C, XM_011531705.2:c.616A>C, XM_011531705.1:c.616A>C, XM_011531706.3:c.568A>C, XM_011531706.2:c.568A>C, XM_011531706.1:c.568A>C, NP_004398.1:p.Lys177Gln, NP_001073380.1:p.Lys161Gln, XP_011530007.1:p.Lys206Gln, XP_011530008.1:p.Lys190Gln

Select item 147084708617.

rs1470847086 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:87662477 (GRCh38)
4:88583629 (GRCh37)
Canonical SPDI:: NC_000004.12:87662476:C:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000004.12:g.87662477C>G, NC_000004.11:g.88583629C>G, NG_008988.1:g.17176C>G, NM_004407.4:c.699C>G, NM_004407.3:c.699C>G, NM_001079911.3:c.651C>G, NM_001079911.2:c.651C>G, XM_011531705.3:c.786C>G, XM_011531705.2:c.786C>G, XM_011531705.1:c.786C>G, XM_011531706.3:c.738C>G, XM_011531706.2:c.738C>G, XM_011531706.1:c.738C>G, NP_004398.1:p.Asn233Lys, NP_001073380.1:p.Asn217Lys, XP_011530007.1:p.Asn262Lys, XP_011530008.1:p.Asn246Lys

Select item 146954424518.

rs1469544245 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:87663222 (GRCh38)
4:88584374 (GRCh37)
Canonical SPDI:: NC_000004.12:87663221:A:G
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.87663222A>G, NC_000004.11:g.88584374A>G, NG_008988.1:g.17921A>G, NM_004407.4:c.1444A>G, NM_004407.3:c.1444A>G, NM_001079911.3:c.1396A>G, NM_001079911.2:c.1396A>G, XM_011531705.3:c.1531A>G, XM_011531705.2:c.1531A>G, XM_011531705.1:c.1531A>G, XM_011531706.3:c.1483A>G, XM_011531706.2:c.1483A>G, XM_011531706.1:c.1483A>G, NP_004398.1:p.Lys482Glu, NP_001073380.1:p.Lys466Glu, XP_011530007.1:p.Lys511Glu, XP_011530008.1:p.Lys495Glu

Select item 146943326519.

rs1469433265 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:87662468 (GRCh38)
4:88583620 (GRCh37)
Canonical SPDI:: NC_000004.12:87662467:C:A
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.87662468C>A, NC_000004.11:g.88583620C>A, NG_008988.1:g.17167C>A, NM_004407.4:c.690C>A, NM_004407.3:c.690C>A, NM_001079911.3:c.642C>A, NM_001079911.2:c.642C>A, XM_011531705.3:c.777C>A, XM_011531705.2:c.777C>A, XM_011531705.1:c.777C>A, XM_011531706.3:c.729C>A, XM_011531706.2:c.729C>A, XM_011531706.1:c.729C>A

Select item 146735504420.

rs1467355044 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:87663096 (GRCh38)
4:88584248 (GRCh37)
Canonical SPDI:: NC_000004.12:87663095:G:A
Gene:: DMP1 (Varview), LOC105377323 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.87663096G>A, NC_000004.11:g.88584248G>A, NG_008988.1:g.17795G>A, NM_004407.4:c.1318G>A, NM_004407.3:c.1318G>A, NM_001079911.3:c.1270G>A, NM_001079911.2:c.1270G>A, XM_011531705.3:c.1405G>A, XM_011531705.2:c.1405G>A, XM_011531705.1:c.1405G>A, XM_011531706.3:c.1357G>A, XM_011531706.2:c.1357G>A, XM_011531706.1:c.1357G>A, NP_004398.1:p.Ala440Thr, NP_001073380.1:p.Ala424Thr, XP_011530007.1:p.Ala469Thr, XP_011530008.1:p.Ala453Thr

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