SNP Links for Protein (Select 30410803) - SNP

Links from Protein

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Select item 14909872871.

rs1490987287 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:45118420 (GRCh38)
3:45159912 (GRCh37)
Canonical SPDI:: NC_000003.12:45118419:T:C
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.45118420T>C, NC_000003.11:g.45159912T>C, NM_022842.5:c.284A>G, NM_022842.4:c.284A>G, NM_178181.3:c.284A>G, NM_178181.2:c.284A>G, XM_011534024.2:c.281A>G, XM_011534024.1:c.281A>G, XM_024453718.2:c.86A>G, XM_024453718.1:c.86A>G, XM_017007070.2:c.284A>G, XM_017007070.1:c.284A>G, XM_047448759.1:c.86A>G, NP_073753.3:p.Lys95Arg, NP_835488.1:p.Lys95Arg, XP_011532326.1:p.Lys94Arg, XP_024309486.1:p.Lys29Arg, XP_016862559.1:p.Lys95Arg, XP_047304715.1:p.Lys29Arg

Select item 14909015782.

rs1490901578 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:45110693 (GRCh38)
3:45152185 (GRCh37)
Canonical SPDI:: NC_000003.12:45110692:G:A
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.45110693G>A, NC_000003.11:g.45152185G>A, NM_022842.5:c.804C>T, NM_022842.4:c.804C>T, NM_178181.3:c.804C>T, NM_178181.2:c.804C>T, XM_011534024.2:c.801C>T, XM_011534024.1:c.801C>T, XM_024453718.2:c.606C>T, XM_024453718.1:c.606C>T, XM_017007070.2:c.804C>T, XM_017007070.1:c.804C>T, XM_047448759.1:c.606C>T

Select item 14886739643.

rs1488673964 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:45110679 (GRCh38)
3:45152171 (GRCh37)
Canonical SPDI:: NC_000003.12:45110678:T:C
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.45110679T>C, NC_000003.11:g.45152171T>C, NM_022842.5:c.818A>G, NM_022842.4:c.818A>G, NM_178181.3:c.818A>G, NM_178181.2:c.818A>G, XM_011534024.2:c.815A>G, XM_011534024.1:c.815A>G, XM_024453718.2:c.620A>G, XM_024453718.1:c.620A>G, XM_017007070.2:c.818A>G, XM_017007070.1:c.818A>G, XM_047448759.1:c.620A>G, NP_073753.3:p.Asn273Ser, NP_835488.1:p.Asn273Ser, XP_011532326.1:p.Asn272Ser, XP_024309486.1:p.Asn207Ser, XP_016862559.1:p.Asn273Ser, XP_047304715.1:p.Asn207Ser

Select item 14847399364.

rs1484739936 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:45112387 (GRCh38)
3:45153879 (GRCh37)
Canonical SPDI:: NC_000003.12:45112386:C:A
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.45112387C>A, NC_000003.11:g.45153879C>A, NM_022842.5:c.351G>T, NM_022842.4:c.351G>T, NM_178181.3:c.351G>T, NM_178181.2:c.351G>T, XM_011534024.2:c.348G>T, XM_011534024.1:c.348G>T, XM_024453718.2:c.153G>T, XM_024453718.1:c.153G>T, XM_017007070.2:c.351G>T, XM_017007070.1:c.351G>T, XM_047448759.1:c.153G>T, NP_073753.3:p.Leu117Phe, NP_835488.1:p.Leu117Phe, XP_011532326.1:p.Leu116Phe, XP_024309486.1:p.Leu51Phe, XP_016862559.1:p.Leu117Phe, XP_047304715.1:p.Leu51Phe

Select item 14844789705.

rs1484478970 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45146230 (GRCh38)
3:45187722 (GRCh37)
Canonical SPDI:: NC_000003.12:45146229:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant,5_prime_UTR_variant
HGVS:: NC_000003.12:g.45146230C>T, NC_000003.11:g.45187722C>T, NM_022842.5:c.58G>A, NM_022842.4:c.58G>A, NM_178181.3:c.58G>A, NM_178181.2:c.58G>A, XM_011534024.2:c.58G>A, XM_011534024.1:c.58G>A, XM_017007070.2:c.58G>A, XM_017007070.1:c.58G>A, XM_047448759.1:c.-197G>A, NP_073753.3:p.Ala20Thr, NP_835488.1:p.Ala20Thr, XP_011532326.1:p.Ala20Thr, XP_016862559.1:p.Ala20Thr

Select item 14822955756.

rs1482295575 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:45118532 (GRCh38)
3:45160024 (GRCh37)
Canonical SPDI:: NC_000003.12:45118531:T:C
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000003.12:g.45118532T>C, NC_000003.11:g.45160024T>C, NM_022842.5:c.172A>G, NM_022842.4:c.172A>G, NM_178181.3:c.172A>G, NM_178181.2:c.172A>G, XM_011534024.2:c.169A>G, XM_011534024.1:c.169A>G, XM_024453718.2:c.-27A>G, XM_024453718.1:c.-27A>G, XM_017007070.2:c.172A>G, XM_017007070.1:c.172A>G, XM_047448759.1:c.-27A>G, NP_073753.3:p.Ile58Val, NP_835488.1:p.Ile58Val, XP_011532326.1:p.Ile57Val, XP_016862559.1:p.Ile58Val

Select item 14806531067.

rs1480653106 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45118436 (GRCh38)
3:45159928 (GRCh37)
Canonical SPDI:: NC_000003.12:45118435:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.45118436C>T, NC_000003.11:g.45159928C>T, NM_022842.5:c.268G>A, NM_022842.4:c.268G>A, NM_178181.3:c.268G>A, NM_178181.2:c.268G>A, XM_011534024.2:c.265G>A, XM_011534024.1:c.265G>A, XM_024453718.2:c.70G>A, XM_024453718.1:c.70G>A, XM_017007070.2:c.268G>A, XM_017007070.1:c.268G>A, XM_047448759.1:c.70G>A, NP_073753.3:p.Val90Ile, NP_835488.1:p.Val90Ile, XP_011532326.1:p.Val89Ile, XP_024309486.1:p.Val24Ile, XP_016862559.1:p.Val90Ile, XP_047304715.1:p.Val24Ile

Select item 14787081078.

rs1478708107 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 3:45112443 (GRCh38)
3:45153935 (GRCh37)
Canonical SPDI:: NC_000003.12:45112442:A:C,NC_000003.12:45112442:A:G
Gene:: CDCP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.45112443A>C, NC_000003.12:g.45112443A>G, NC_000003.11:g.45153935A>C, NC_000003.11:g.45153935A>G, NM_022842.5:c.295T>G, NM_022842.5:c.295T>C, NM_022842.4:c.295T>G, NM_022842.4:c.295T>C, NM_178181.3:c.295T>G, NM_178181.3:c.295T>C, NM_178181.2:c.295T>G, NM_178181.2:c.295T>C, XM_011534024.2:c.292T>G, XM_011534024.2:c.292T>C, XM_011534024.1:c.292T>G, XM_011534024.1:c.292T>C, XM_024453718.2:c.97T>G, XM_024453718.2:c.97T>C, XM_024453718.1:c.97T>G, XM_024453718.1:c.97T>C, XM_017007070.2:c.295T>G, XM_017007070.2:c.295T>C, XM_017007070.1:c.295T>G, XM_017007070.1:c.295T>C, XM_047448759.1:c.97T>G, XM_047448759.1:c.97T>C, NP_073753.3:p.Cys99Gly, NP_073753.3:p.Cys99Arg, NP_835488.1:p.Cys99Gly, NP_835488.1:p.Cys99Arg, XP_011532326.1:p.Cys98Gly, XP_011532326.1:p.Cys98Arg, XP_024309486.1:p.Cys33Gly, XP_024309486.1:p.Cys33Arg, XP_016862559.1:p.Cys99Gly, XP_016862559.1:p.Cys99Arg, XP_047304715.1:p.Cys33Gly, XP_047304715.1:p.Cys33Arg

Select item 14767300239.

rs1476730023 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45110594 (GRCh38)
3:45152086 (GRCh37)
Canonical SPDI:: NC_000003.12:45110593:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.45110594C>T, NC_000003.11:g.45152086C>T, NM_022842.5:c.903G>A, NM_022842.4:c.903G>A, NM_178181.3:c.903G>A, NM_178181.2:c.903G>A, XM_011534024.2:c.900G>A, XM_011534024.1:c.900G>A, XM_024453718.2:c.705G>A, XM_024453718.1:c.705G>A, XM_017007070.2:c.903G>A, XM_017007070.1:c.903G>A, XM_047448759.1:c.705G>A

Select item 147625449110.

rs1476254491 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:45118600 (GRCh38)
3:45160092 (GRCh37)
Canonical SPDI:: NC_000003.12:45118599:G:T
Gene:: CDCP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.45118600G>T, NC_000003.11:g.45160092G>T, NM_022842.5:c.104C>A, NM_022842.4:c.104C>A, NM_178181.3:c.104C>A, NM_178181.2:c.104C>A, XM_011534024.2:c.101C>A, XM_011534024.1:c.101C>A, XM_024453718.2:c.-95C>A, XM_024453718.1:c.-95C>A, XM_017007070.2:c.104C>A, XM_017007070.1:c.104C>A, XM_047448759.1:c.-95C>A, NP_073753.3:p.Pro35Gln, NP_835488.1:p.Pro35Gln, XP_011532326.1:p.Pro34Gln, XP_016862559.1:p.Pro35Gln

Select item 147247130411.

rs1472471304 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 3:45112408 (GRCh38)
3:45153900 (GRCh37)
Canonical SPDI:: NC_000003.12:45112407:C:A,NC_000003.12:45112407:C:G
Gene:: CDCP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
G=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.45112408C>A, NC_000003.12:g.45112408C>G, NC_000003.11:g.45153900C>A, NC_000003.11:g.45153900C>G, NM_022842.5:c.330G>T, NM_022842.5:c.330G>C, NM_022842.4:c.330G>T, NM_022842.4:c.330G>C, NM_178181.3:c.330G>T, NM_178181.3:c.330G>C, NM_178181.2:c.330G>T, NM_178181.2:c.330G>C, XM_011534024.2:c.327G>T, XM_011534024.2:c.327G>C, XM_011534024.1:c.327G>T, XM_011534024.1:c.327G>C, XM_024453718.2:c.132G>T, XM_024453718.2:c.132G>C, XM_024453718.1:c.132G>T, XM_024453718.1:c.132G>C, XM_017007070.2:c.330G>T, XM_017007070.2:c.330G>C, XM_017007070.1:c.330G>T, XM_017007070.1:c.330G>C, XM_047448759.1:c.132G>T, XM_047448759.1:c.132G>C, NP_073753.3:p.Gln110His, NP_073753.3:p.Gln110His, NP_835488.1:p.Gln110His, NP_835488.1:p.Gln110His, XP_011532326.1:p.Gln109His, XP_011532326.1:p.Gln109His, XP_024309486.1:p.Gln44His, XP_024309486.1:p.Gln44His, XP_016862559.1:p.Gln110His, XP_016862559.1:p.Gln110His, XP_047304715.1:p.Gln44His, XP_047304715.1:p.Gln44His

Select item 146508780812.

rs1465087808 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:45118414 (GRCh38)
3:45159906 (GRCh37)
Canonical SPDI:: NC_000003.12:45118413:A:G
Gene:: CDCP1 (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_000003.12:g.45118414A>G, NC_000003.11:g.45159906A>G, NM_022842.5:c.290T>C, NM_022842.4:c.290T>C, NM_178181.3:c.290T>C, NM_178181.2:c.290T>C, XM_011534024.2:c.287T>C, XM_011534024.1:c.287T>C, XM_024453718.2:c.92T>C, XM_024453718.1:c.92T>C, XM_017007070.2:c.290T>C, XM_017007070.1:c.290T>C, XM_047448759.1:c.92T>C, NP_073753.3:p.Ile97Thr, NP_835488.1:p.Ile97Thr, XP_011532326.1:p.Ile96Thr, XP_024309486.1:p.Ile31Thr, XP_016862559.1:p.Ile97Thr, XP_047304715.1:p.Ile31Thr

Select item 146486365513.

rs1464863655 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:45112144 (GRCh38)
3:45153636 (GRCh37)
Canonical SPDI:: NC_000003.12:45112143:G:C
Gene:: CDCP1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.45112144G>C, NC_000003.11:g.45153636G>C, NM_022842.5:c.594C>G, NM_022842.4:c.594C>G, NM_178181.3:c.594C>G, NM_178181.2:c.594C>G, XM_011534024.2:c.591C>G, XM_011534024.1:c.591C>G, XM_024453718.2:c.396C>G, XM_024453718.1:c.396C>G, XM_017007070.2:c.594C>G, XM_017007070.1:c.594C>G, XM_047448759.1:c.396C>G

Select item 145668985014.

rs1456689850 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:45146245 (GRCh38)
3:45187737 (GRCh37)
Canonical SPDI:: NC_000003.12:45146244:C:A
Gene:: CDCP1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.45146245C>A, NC_000003.11:g.45187737C>A, NM_022842.5:c.43G>T, NM_022842.4:c.43G>T, NM_178181.3:c.43G>T, NM_178181.2:c.43G>T, XM_011534024.2:c.43G>T, XM_011534024.1:c.43G>T, XM_017007070.2:c.43G>T, XM_017007070.1:c.43G>T, XM_047448759.1:c.-212G>T, NP_073753.3:p.Val15Phe, NP_835488.1:p.Val15Phe, XP_011532326.1:p.Val15Phe, XP_016862559.1:p.Val15Phe

Select item 144670722215.

rs1446707222 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45110510 (GRCh38)
3:45152002 (GRCh37)
Canonical SPDI:: NC_000003.12:45110509:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.45110510C>T, NC_000003.11:g.45152002C>T, NM_022842.5:c.987G>A, NM_022842.4:c.987G>A, NM_178181.3:c.987G>A, NM_178181.2:c.987G>A, XM_011534024.2:c.984G>A, XM_011534024.1:c.984G>A, XM_024453718.2:c.789G>A, XM_024453718.1:c.789G>A, XM_017007070.2:c.987G>A, XM_017007070.1:c.987G>A, XM_047448759.1:c.789G>A

Select item 144207932316.

rs1442079323 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:45112235 (GRCh38)
3:45153727 (GRCh37)
Canonical SPDI:: NC_000003.12:45112234:T:G
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.45112235T>G, NC_000003.11:g.45153727T>G, NM_022842.5:c.503A>C, NM_022842.4:c.503A>C, NM_178181.3:c.503A>C, NM_178181.2:c.503A>C, XM_011534024.2:c.500A>C, XM_011534024.1:c.500A>C, XM_024453718.2:c.305A>C, XM_024453718.1:c.305A>C, XM_017007070.2:c.503A>C, XM_017007070.1:c.503A>C, XM_047448759.1:c.305A>C, NP_073753.3:p.Asp168Ala, NP_835488.1:p.Asp168Ala, XP_011532326.1:p.Asp167Ala, XP_024309486.1:p.Asp102Ala, XP_016862559.1:p.Asp168Ala, XP_047304715.1:p.Asp102Ala

Select item 144023442417.

rs1440234424 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45110792 (GRCh38)
3:45152284 (GRCh37)
Canonical SPDI:: NC_000003.12:45110791:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.45110792C>T, NC_000003.11:g.45152284C>T, NM_022842.5:c.705G>A, NM_022842.4:c.705G>A, NM_178181.3:c.705G>A, NM_178181.2:c.705G>A, XM_011534024.2:c.702G>A, XM_011534024.1:c.702G>A, XM_024453718.2:c.507G>A, XM_024453718.1:c.507G>A, XM_017007070.2:c.705G>A, XM_017007070.1:c.705G>A, XM_047448759.1:c.507G>A

Select item 143899592218.

rs1438995922 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:45118483 (GRCh38)
3:45159975 (GRCh37)
Canonical SPDI:: NC_000003.12:45118482:T:C
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000003.12:g.45118483T>C, NC_000003.11:g.45159975T>C, NM_022842.5:c.221A>G, NM_022842.4:c.221A>G, NM_178181.3:c.221A>G, NM_178181.2:c.221A>G, XM_011534024.2:c.218A>G, XM_011534024.1:c.218A>G, XM_024453718.2:c.23A>G, XM_024453718.1:c.23A>G, XM_017007070.2:c.221A>G, XM_017007070.1:c.221A>G, XM_047448759.1:c.23A>G, NP_073753.3:p.Glu74Gly, NP_835488.1:p.Glu74Gly, XP_011532326.1:p.Glu73Gly, XP_024309486.1:p.Glu8Gly, XP_016862559.1:p.Glu74Gly, XP_047304715.1:p.Glu8Gly

Select item 143847413019.

rs1438474130 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:45146229 (GRCh38)
3:45187721 (GRCh37)
Canonical SPDI:: NC_000003.12:45146228:G:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.45146229G>T, NC_000003.11:g.45187721G>T, NM_022842.5:c.59C>A, NM_022842.4:c.59C>A, NM_178181.3:c.59C>A, NM_178181.2:c.59C>A, XM_011534024.2:c.59C>A, XM_011534024.1:c.59C>A, XM_017007070.2:c.59C>A, XM_017007070.1:c.59C>A, XM_047448759.1:c.-196C>A, NP_073753.3:p.Ala20Glu, NP_835488.1:p.Ala20Glu, XP_011532326.1:p.Ala20Glu, XP_016862559.1:p.Ala20Glu

Select item 142914601920.

rs1429146019 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:45112318 (GRCh38)
3:45153810 (GRCh37)
Canonical SPDI:: NC_000003.12:45112317:C:T
Gene:: CDCP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.45112318C>T, NC_000003.11:g.45153810C>T, NM_022842.5:c.420G>A, NM_022842.4:c.420G>A, NM_178181.3:c.420G>A, NM_178181.2:c.420G>A, XM_011534024.2:c.417G>A, XM_011534024.1:c.417G>A, XM_024453718.2:c.222G>A, XM_024453718.1:c.222G>A, XM_017007070.2:c.420G>A, XM_017007070.1:c.420G>A, XM_047448759.1:c.222G>A

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