SNP Links for Protein (Select 23308597) - SNP

Links from Protein

Items: 1 to 20 of 543

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Select item 14871372301.

rs1487137230 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:10487835 (GRCh38)
18:10487832 (GRCh37)
Canonical SPDI:: NC_000018.10:10487834:A:G
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10487835A>G, NC_000018.9:g.10487832A>G, NG_027685.1:g.38208A>G, NM_153000.5:c.1342A>G, NM_153000.4:c.1342A>G, XM_047437309.1:c.727A>G, NP_694545.1:p.Ser448Gly, XP_047293265.1:p.Ser243Gly

Select item 14854255312.

rs1485425531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:10471593 (GRCh38)
18:10471590 (GRCh37)
Canonical SPDI:: NC_000018.10:10471592:C:T
Gene:: APCDD1 (Varview)
Functional Consequence:: synonymous_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=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.10471593C>T, NC_000018.9:g.10471590C>T, NG_027685.1:g.21966C>T, NM_153000.5:c.306C>T, NM_153000.4:c.306C>T, XM_011525603.3:c.306C>T, XM_011525603.2:c.306C>T, XM_011525603.1:c.306C>T, XM_047437309.1:c.-310C>T

Select item 14833023953.

rs1483302395 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:10471581 (GRCh38)
18:10471578 (GRCh37)
Canonical SPDI:: NC_000018.10:10471580:C:T
Gene:: APCDD1 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10471581C>T, NC_000018.9:g.10471578C>T, NG_027685.1:g.21954C>T, NM_153000.5:c.294C>T, NM_153000.4:c.294C>T, XM_011525603.3:c.294C>T, XM_011525603.2:c.294C>T, XM_011525603.1:c.294C>T, XM_047437309.1:c.-322C>T

Select item 14832812594.

rs1483281259 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:10485708 (GRCh38)
18:10485705 (GRCh37)
Canonical SPDI:: NC_000018.10:10485707:A:G
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.10485708A>G, NC_000018.9:g.10485705A>G, NG_027685.1:g.36081A>G, NM_153000.5:c.1021A>G, NM_153000.4:c.1021A>G, XM_047437309.1:c.406A>G, NP_694545.1:p.Ile341Val, XP_047293265.1:p.Ile136Val

Select item 14830663245.

rs1483066324 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 18:10487763 (GRCh38)
18:10487760 (GRCh37)
Canonical SPDI:: NC_000018.10:10487762:A:G,NC_000018.10:10487762:A:T
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.10487763A>G, NC_000018.10:g.10487763A>T, NC_000018.9:g.10487760A>G, NC_000018.9:g.10487760A>T, NG_027685.1:g.38136A>G, NG_027685.1:g.38136A>T, NM_153000.5:c.1270A>G, NM_153000.5:c.1270A>T, NM_153000.4:c.1270A>G, NM_153000.4:c.1270A>T, XM_047437309.1:c.655A>G, XM_047437309.1:c.655A>T, NP_694545.1:p.Ile424Val, NP_694545.1:p.Ile424Phe, XP_047293265.1:p.Ile219Val, XP_047293265.1:p.Ile219Phe

Select item 14786078376.

rs1478607837 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:10471746 (GRCh38)
18:10471743 (GRCh37)
Canonical SPDI:: NC_000018.10:10471745:C:G
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10471746C>G, NC_000018.9:g.10471743C>G, NG_027685.1:g.22119C>G, NM_153000.5:c.459C>G, NM_153000.4:c.459C>G, XM_011525603.3:c.459C>G, XM_011525603.2:c.459C>G, XM_011525603.1:c.459C>G, XM_047437309.1:c.-157C>G, NP_694545.1:p.Ile153Met, XP_011523905.1:p.Ile153Met

Select item 14775878787.

rs1477587878 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:10468585 (GRCh38)
18:10468582 (GRCh37)
Canonical SPDI:: NC_000018.10:10468584:C:A
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_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_000018.10:g.10468585C>A, NC_000018.9:g.10468582C>A, NG_027685.1:g.18958C>A, NM_153000.5:c.175C>A, NM_153000.4:c.175C>A, XM_011525603.3:c.175C>A, XM_011525603.2:c.175C>A, XM_011525603.1:c.175C>A, NP_694545.1:p.Leu59Ile, XP_011523905.1:p.Leu59Ile

Select item 14771100568.

rs1477110056 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:10485777 (GRCh38)
18:10485774 (GRCh37)
Canonical SPDI:: NC_000018.10:10485776:T:C
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
HGVS:: NC_000018.10:g.10485777T>C, NC_000018.9:g.10485774T>C, NG_027685.1:g.36150T>C, NM_153000.5:c.1090T>C, NM_153000.4:c.1090T>C, XM_047437309.1:c.475T>C, NP_694545.1:p.Phe364Leu, XP_047293265.1:p.Phe159Leu

Select item 14718297159.

rs1471829715 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 18:10471946 (GRCh38)
18:10471943 (GRCh37)
Canonical SPDI:: NC_000018.10:10471945:A:C
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000018.10:g.10471946A>C, NC_000018.9:g.10471943A>C, NG_027685.1:g.22319A>C, NM_153000.5:c.659A>C, NM_153000.4:c.659A>C, XM_011525603.3:c.659A>C, XM_011525603.2:c.659A>C, XM_011525603.1:c.659A>C, XM_047437309.1:c.44A>C, NP_694545.1:p.His220Pro, XP_011523905.1:p.His220Pro, XP_047293265.1:p.His15Pro

Select item 147001643810.

rs1470016438 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:10454993 (GRCh38)
18:10454990 (GRCh37)
Canonical SPDI:: NC_000018.10:10454992:G:A
Gene:: APCDD1 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
HGVS:: NC_000018.10:g.10454993G>A, NC_000018.9:g.10454990G>A, NG_027685.1:g.5366G>A, NM_153000.5:c.12G>A, NM_153000.4:c.12G>A, XM_011525603.3:c.12G>A, XM_011525603.2:c.12G>A, XM_011525603.1:c.12G>A, XM_047437309.1:c.-420G>A

Select item 146916707411.

rs1469167074 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 18:10454987 (GRCh38)
18:10454984 (GRCh37)
Canonical SPDI:: NC_000018.10:10454986:C:G,NC_000018.10:10454986:C:T
Gene:: APCDD1 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000018.10:g.10454987C>G, NC_000018.10:g.10454987C>T, NC_000018.9:g.10454984C>G, NC_000018.9:g.10454984C>T, NG_027685.1:g.5360C>G, NG_027685.1:g.5360C>T, NM_153000.5:c.6C>G, NM_153000.5:c.6C>T, NM_153000.4:c.6C>G, NM_153000.4:c.6C>T, XM_011525603.3:c.6C>G, XM_011525603.3:c.6C>T, XM_011525603.2:c.6C>G, XM_011525603.2:c.6C>T, XM_011525603.1:c.6C>G, XM_011525603.1:c.6C>T, XM_047437309.1:c.-426C>G, XM_047437309.1:c.-426C>T

Select item 146757886412.

rs1467578864 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:10468562 (GRCh38)
18:10468559 (GRCh37)
Canonical SPDI:: NC_000018.10:10468561:A:G
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.10468562A>G, NC_000018.9:g.10468559A>G, NG_027685.1:g.18935A>G, NM_153000.5:c.152A>G, NM_153000.4:c.152A>G, XM_011525603.3:c.152A>G, XM_011525603.2:c.152A>G, XM_011525603.1:c.152A>G, NP_694545.1:p.Gln51Arg, XP_011523905.1:p.Gln51Arg

Select item 146754595513.

rs1467545955 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:10468542 (GRCh38)
18:10468539 (GRCh37)
Canonical SPDI:: NC_000018.10:10468541:G:C
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10468542G>C, NC_000018.9:g.10468539G>C, NG_027685.1:g.18915G>C, NM_153000.5:c.132G>C, NM_153000.4:c.132G>C, XM_011525603.3:c.132G>C, XM_011525603.2:c.132G>C, XM_011525603.1:c.132G>C, NP_694545.1:p.Trp44Cys, XP_011523905.1:p.Trp44Cys

Select item 146497135014.

rs1464971350 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 18:10487824 (GRCh38)
18:10487821 (GRCh37)
Canonical SPDI:: NC_000018.10:10487823:G:C,NC_000018.10:10487823:G:T
Gene:: APCDD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.10487824G>C, NC_000018.10:g.10487824G>T, NC_000018.9:g.10487821G>C, NC_000018.9:g.10487821G>T, NG_027685.1:g.38197G>C, NG_027685.1:g.38197G>T, NM_153000.5:c.1331G>C, NM_153000.5:c.1331G>T, NM_153000.4:c.1331G>C, NM_153000.4:c.1331G>T, XM_047437309.1:c.716G>C, XM_047437309.1:c.716G>T, NP_694545.1:p.Ser444Thr, NP_694545.1:p.Ser444Ile, XP_047293265.1:p.Ser239Thr, XP_047293265.1:p.Ser239Ile

Select item 145792846315.

rs1457928463 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 18:10487985 (GRCh38)
18:10487982 (GRCh37)
Canonical SPDI:: NC_000018.10:10487984:C:G,NC_000018.10:10487984:C:T
Gene:: APCDD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.10487985C>G, NC_000018.10:g.10487985C>T, NC_000018.9:g.10487982C>G, NC_000018.9:g.10487982C>T, NG_027685.1:g.38358C>G, NG_027685.1:g.38358C>T, NM_153000.5:c.1492C>G, NM_153000.5:c.1492C>T, NM_153000.4:c.1492C>G, NM_153000.4:c.1492C>T, XM_047437309.1:c.877C>G, XM_047437309.1:c.877C>T, NP_694545.1:p.Leu498Val, XP_047293265.1:p.Leu293Val

Select item 145783791216.

rs1457837912 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:10487645 (GRCh38)
18:10487642 (GRCh37)
Canonical SPDI:: NC_000018.10:10487644:C:G
Gene:: APCDD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.10487645C>G, NC_000018.9:g.10487642C>G, NG_027685.1:g.38018C>G, NM_153000.5:c.1152C>G, NM_153000.4:c.1152C>G, XM_047437309.1:c.537C>G

Select item 145531921017.

rs1455319210 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:10485504 (GRCh38)
18:10485501 (GRCh37)
Canonical SPDI:: NC_000018.10:10485503:T:C
Gene:: APCDD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10485504T>C, NC_000018.9:g.10485501T>C, NG_027685.1:g.35877T>C, NM_153000.5:c.817T>C, NM_153000.4:c.817T>C, XM_047437309.1:c.202T>C, NP_694545.1:p.Ser273Pro, XP_047293265.1:p.Ser68Pro

Select item 145487245518.

rs1454872455 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:10485743 (GRCh38)
18:10485740 (GRCh37)
Canonical SPDI:: NC_000018.10:10485742:C:A
Gene:: APCDD1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000018.10:g.10485743C>A, NC_000018.9:g.10485740C>A, NG_027685.1:g.36116C>A, NM_153000.5:c.1056C>A, NM_153000.4:c.1056C>A, XM_047437309.1:c.441C>A

Select item 144896385519.

rs1448963855 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:10471726 (GRCh38)
18:10471723 (GRCh37)
Canonical SPDI:: NC_000018.10:10471725:C:T
Gene:: APCDD1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,synonymous_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_000018.10:g.10471726C>T, NC_000018.9:g.10471723C>T, NG_027685.1:g.22099C>T, NM_153000.5:c.439C>T, NM_153000.4:c.439C>T, XM_011525603.3:c.439C>T, XM_011525603.2:c.439C>T, XM_011525603.1:c.439C>T, XM_047437309.1:c.-177C>T

Select item 144868607920.

rs1448686079 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:10471949 (GRCh38)
18:10471946 (GRCh37)
Canonical SPDI:: NC_000018.10:10471948:A:G
Gene:: APCDD1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.10471949A>G, NC_000018.9:g.10471946A>G, NG_027685.1:g.22322A>G, NM_153000.5:c.662A>G, NM_153000.4:c.662A>G, XM_011525603.3:c.662A>G, XM_011525603.2:c.662A>G, XM_011525603.1:c.662A>G, XM_047437309.1:c.47A>G, NP_694545.1:p.His221Arg, XP_011523905.1:p.His221Arg, XP_047293265.1:p.His16Arg

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