SNP Links for Protein (Select 72384339) - SNP

Links from Protein

Items: 1 to 20 of 516

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Select item 14904828651.

rs1490482865 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54152880 (GRCh38)
1:54618553 (GRCh37)
Canonical SPDI:: NC_000001.11:54152879:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: synonymous_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)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.54152880G>A, NC_000001.10:g.54618553G>A, NM_201546.5:c.43C>T, NM_201546.4:c.43C>T, NM_201546.3:c.43C>T, NM_001353655.3:c.43C>T, NM_001353655.2:c.43C>T, NM_001353655.1:c.43C>T

Select item 14904671742.

rs1490467174 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:54141355 (GRCh38)
1:54607028 (GRCh37)
Canonical SPDI:: NC_000001.11:54141354:A:C,NC_000001.11:54141354:A:G,NC_000001.11:54141354:A:T
Gene:: CDCP2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000001.11:g.54141355A>C, NC_000001.11:g.54141355A>G, NC_000001.11:g.54141355A>T, NC_000001.10:g.54607028A>C, NC_000001.10:g.54607028A>G, NC_000001.10:g.54607028A>T, NM_201546.5:c.506T>G, NM_201546.5:c.506T>C, NM_201546.5:c.506T>A, NM_201546.4:c.506T>G, NM_201546.4:c.506T>C, NM_201546.4:c.506T>A, NM_201546.3:c.506T>G, NM_201546.3:c.506T>C, NM_201546.3:c.506T>A, NM_001353655.3:c.506T>G, NM_001353655.3:c.506T>C, NM_001353655.3:c.506T>A, NM_001353655.2:c.506T>G, NM_001353655.2:c.506T>C, NM_001353655.2:c.506T>A, NM_001353655.1:c.506T>G, NM_001353655.1:c.506T>C, NM_001353655.1:c.506T>A, NP_963840.2:p.Met169Arg, NP_963840.2:p.Met169Thr, NP_963840.2:p.Met169Lys, NP_001340584.1:p.Met169Arg, NP_001340584.1:p.Met169Thr, NP_001340584.1:p.Met169Lys

Select item 14887434293.

rs1488743429 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54139963 (GRCh38)
1:54605636 (GRCh37)
Canonical SPDI:: NC_000001.11:54139962:C:T
Gene:: CDCP2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.54139963C>T, NC_000001.10:g.54605636C>T, NM_201546.5:c.907G>A, NM_201546.4:c.907G>A, NM_201546.3:c.907G>A, NM_001353655.3:c.907G>A, NM_001353655.2:c.907G>A, NM_001353655.1:c.907G>A, NP_963840.2:p.Asp303Asn, NP_001340584.1:p.Asp303Asn

Select item 14884177734.

rs1488417773 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:54144655 (GRCh38)
1:54610328 (GRCh37)
Canonical SPDI:: NC_000001.11:54144654:G:T
Gene:: CDCP2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54144655G>T, NC_000001.10:g.54610328G>T, NM_201546.5:c.238C>A, NM_201546.4:c.238C>A, NM_201546.3:c.238C>A, NM_001353655.3:c.238C>A, NM_001353655.2:c.238C>A, NM_001353655.1:c.238C>A, NP_963840.2:p.His80Asn, NP_001340584.1:p.His80Asn

Select item 14865985125.

rs1486598512 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54152890 (GRCh38)
1:54618563 (GRCh37)
Canonical SPDI:: NC_000001.11:54152889:C:T
Gene:: CDCP2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54152890C>T, NC_000001.10:g.54618563C>T, NM_201546.5:c.33G>A, NM_201546.4:c.33G>A, NM_201546.3:c.33G>A, NM_001353655.3:c.33G>A, NM_001353655.2:c.33G>A, NM_001353655.1:c.33G>A

Select item 14864429566.

rs1486442956 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:54141161 (GRCh38)
1:54606834 (GRCh37)
Canonical SPDI:: NC_000001.11:54141160:G:A,NC_000001.11:54141160:G:T
Gene:: CDCP2 (Varview)
Functional Consequence:: missense_variant,stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54141161G>A, NC_000001.11:g.54141161G>T, NC_000001.10:g.54606834G>A, NC_000001.10:g.54606834G>T, NM_201546.5:c.700C>T, NM_201546.5:c.700C>A, NM_201546.4:c.700C>T, NM_201546.4:c.700C>A, NM_201546.3:c.700C>T, NM_201546.3:c.700C>A, NM_001353655.3:c.700C>T, NM_001353655.3:c.700C>A, NM_001353655.2:c.700C>T, NM_001353655.2:c.700C>A, NM_001353655.1:c.700C>T, NM_001353655.1:c.700C>A, NP_963840.2:p.Gln234Ter, NP_963840.2:p.Gln234Lys, NP_001340584.1:p.Gln234Ter, NP_001340584.1:p.Gln234Lys

Select item 14844735697.

rs1484473569 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54139630 (GRCh38)
1:54605303 (GRCh37)
Canonical SPDI:: NC_000001.11:54139629:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: intron_variant,stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.54139630G>A, NC_000001.10:g.54605303G>A, NM_201546.5:c.1240C>T, NM_201546.4:c.1240C>T, NM_201546.3:c.1240C>T, NP_963840.2:p.Gln414Ter

Select item 14822516568.

rs1482251656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54141281 (GRCh38)
1:54606954 (GRCh37)
Canonical SPDI:: NC_000001.11:54141280:C:T
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000001.11:g.54141281C>T, NC_000001.10:g.54606954C>T, NM_201546.5:c.580G>A, NM_201546.4:c.580G>A, NM_201546.3:c.580G>A, NM_001353655.3:c.580G>A, NM_001353655.2:c.580G>A, NM_001353655.1:c.580G>A, NP_963840.2:p.Gly194Ser, NP_001340584.1:p.Gly194Ser

Select item 14805513079.

rs1480551307 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:54141263 (GRCh38)
1:54606936 (GRCh37)
Canonical SPDI:: NC_000001.11:54141262:A:T
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.54141263A>T, NC_000001.10:g.54606936A>T, NM_201546.5:c.598T>A, NM_201546.4:c.598T>A, NM_201546.3:c.598T>A, NM_001353655.3:c.598T>A, NM_001353655.2:c.598T>A, NM_001353655.1:c.598T>A, NP_963840.2:p.Tyr200Asn, NP_001340584.1:p.Tyr200Asn

Select item 147703663010.

rs1477036630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54144789 (GRCh38)
1:54610462 (GRCh37)
Canonical SPDI:: NC_000001.11:54144788:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.54144789G>A, NC_000001.10:g.54610462G>A, NM_201546.5:c.104C>T, NM_201546.4:c.104C>T, NM_201546.3:c.104C>T, NM_001353655.3:c.104C>T, NM_001353655.2:c.104C>T, NM_001353655.1:c.104C>T, NP_963840.2:p.Ser35Leu, NP_001340584.1:p.Ser35Leu

Select item 147583746011.

rs1475837460 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:54144593 (GRCh38)
1:54610266 (GRCh37)
Canonical SPDI:: NC_000001.11:54144592:G:T
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54144593G>T, NC_000001.10:g.54610266G>T, NM_201546.5:c.300C>A, NM_201546.4:c.300C>A, NM_201546.3:c.300C>A, NM_001353655.3:c.300C>A, NM_001353655.2:c.300C>A, NM_001353655.1:c.300C>A, NP_963840.2:p.Asn100Lys, NP_001340584.1:p.Asn100Lys

Select item 146800017312.

rs1468000173 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:54139916 (GRCh38)
1:54605589 (GRCh37)
Canonical SPDI:: NC_000001.11:54139915:A:G
Gene:: CDCP2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000001.11:g.54139916A>G, NC_000001.10:g.54605589A>G, NM_201546.5:c.954T>C, NM_201546.4:c.954T>C, NM_201546.3:c.954T>C, NM_001353655.3:c.954T>C, NM_001353655.2:c.954T>C, NM_001353655.1:c.954T>C

Select item 146755024413.

rs1467550244 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:54139701 (GRCh38)
1:54605374 (GRCh37)
Canonical SPDI:: NC_000001.11:54139700:T:C
Gene:: CDCP2 (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=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.54139701T>C, NC_000001.10:g.54605374T>C, NM_201546.5:c.1169A>G, NM_201546.4:c.1169A>G, NM_201546.3:c.1169A>G, NP_963840.2:p.Gln390Arg

Select item 146713139914.

rs1467131399 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54139823 (GRCh38)
1:54605496 (GRCh37)
Canonical SPDI:: NC_000001.11:54139822:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.54139823G>A, NC_000001.10:g.54605496G>A, NM_201546.5:c.1047C>T, NM_201546.4:c.1047C>T, NM_201546.3:c.1047C>T, NM_001353655.3:c.1047C>T, NM_001353655.2:c.1047C>T, NM_001353655.1:c.1047C>T

Select item 146622220515.

rs1466222205 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54140098 (GRCh38)
1:54605771 (GRCh37)
Canonical SPDI:: NC_000001.11:54140097:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.54140098G>A, NC_000001.10:g.54605771G>A, NM_201546.5:c.772C>T, NM_201546.4:c.772C>T, NM_201546.3:c.772C>T, NM_001353655.3:c.772C>T, NM_001353655.2:c.772C>T, NM_001353655.1:c.772C>T, NP_963840.2:p.Gln258Ter, NP_001340584.1:p.Gln258Ter

Select item 146347961216.

rs1463479612 [Homo sapiens]

Variant type:: DELINS
Alleles:: GTCCAGTGGCAGCGGATG>- [Show Flanks]
Chromosome:: 1:54140013 (GRCh38)
1:54605686 (GRCh37)
Canonical SPDI:: NC_000001.11:54140005:GCGGATGGTCCAGTGGCAGCGGATG:GCGGATG
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
Validated:: by frequency,by alfa
MAF:: GCGGATG=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.54140013_54140030del, NC_000001.10:g.54605686_54605703del, NM_201546.5:c.847_864del, NM_201546.4:c.847_864del, NM_201546.3:c.847_864del, NM_001353655.3:c.847_864del, NM_001353655.2:c.847_864del, NM_001353655.1:c.847_864del, NP_963840.2:p.Cys283_Arg288del, NP_001340584.1:p.Cys283_Arg288del

Select item 146003673517.

rs1460036735 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54139790 (GRCh38)
1:54605463 (GRCh37)
Canonical SPDI:: NC_000001.11:54139789:G:A
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54139790G>A, NC_000001.10:g.54605463G>A, NM_201546.5:c.1080C>T, NM_201546.4:c.1080C>T, NM_201546.3:c.1080C>T, NM_001353655.3:c.1080C>T, NM_001353655.2:c.1080C>T, NM_001353655.1:c.1080C>T

Select item 145611369518.

rs1456113695 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54144479 (GRCh38)
1:54610152 (GRCh37)
Canonical SPDI:: NC_000001.11:54144478:C:T
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54144479C>T, NC_000001.10:g.54610152C>T, NM_201546.5:c.414G>A, NM_201546.4:c.414G>A, NM_201546.3:c.414G>A, NM_001353655.3:c.414G>A, NM_001353655.2:c.414G>A, NM_001353655.1:c.414G>A

Select item 145288859519.

rs1452888595 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:54144783 (GRCh38)
1:54610456 (GRCh37)
Canonical SPDI:: NC_000001.11:54144782:G:C
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54144783G>C, NC_000001.10:g.54610456G>C, NM_201546.5:c.110C>G, NM_201546.4:c.110C>G, NM_201546.3:c.110C>G, NM_001353655.3:c.110C>G, NM_001353655.2:c.110C>G, NM_001353655.1:c.110C>G, NP_963840.2:p.Pro37Arg, NP_001340584.1:p.Pro37Arg

Select item 145216038720.

rs1452160387 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:54144488 (GRCh38)
1:54610161 (GRCh37)
Canonical SPDI:: NC_000001.11:54144487:G:C,NC_000001.11:54144487:G:T
Gene:: CDCP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
T=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.54144488G>C, NC_000001.11:g.54144488G>T, NC_000001.10:g.54610161G>C, NC_000001.10:g.54610161G>T, NM_201546.5:c.405C>G, NM_201546.5:c.405C>A, NM_201546.4:c.405C>G, NM_201546.4:c.405C>A, NM_201546.3:c.405C>G, NM_201546.3:c.405C>A, NM_001353655.3:c.405C>G, NM_001353655.3:c.405C>A, NM_001353655.2:c.405C>G, NM_001353655.2:c.405C>A, NM_001353655.1:c.405C>G, NM_001353655.1:c.405C>A

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