Variant #0000994707 (NC_000005.9:g.140307379C>T, NC_000005.9(NM_018900.2):c.2395-51155C>T (PCDHA1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.140307379C>T
DNA change (hg38) -
Published as PCDHAC1(NM_018898.3):c.902C>T (p.(Pro301Leu))
ISCN -
DB-ID PCDHA1_000074
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PCDHAC1 NM_018898.3 -?/. - c.902C>T r.(?) p.(Pro301Leu)
PCDHAC2 NM_018899.5 -?/. - c.-38973C>T r.(?) p.(=)
PCDHA1 NM_018900.2 -?/. - c.2395-51155C>T r.(=) p.(=)
PCDHA10 NM_018901.2 -?/. - c.2389-51155C>T r.(=) p.(=)
PCDHA11 NM_018902.3 -?/. - c.2392-51155C>T r.(=) p.(=)
PCDHA12 NM_018903.2 -?/. - c.2367+49955C>T r.(=) p.(=)
PCDHA13 NM_018904.2 -?/. - c.2394+43132C>T r.(=) p.(=)
PCDHA2 NM_018905.2 -?/. - c.2389-51155C>T r.(=) p.(=)
PCDHA3 NM_018906.2 -?/. - c.2395-51155C>T r.(=) p.(=)
PCDHA4 NM_018907.2 -?/. - c.2386-51155C>T r.(=) p.(=)
PCDHA5 NM_018908.2 -?/. - c.2353-51155C>T r.(=) p.(=)
PCDHA6 NM_018909.2 -?/. - c.2395-51155C>T r.(=) p.(=)
PCDHA7 NM_018910.2 -?/. - c.2356-51155C>T r.(=) p.(=)
PCDHA8 NM_018911.2 -?/. - c.2395-51155C>T r.(=) p.(=)
PCDHA9 NM_031857.1 -?/. - c.2395-51155C>T r.(=) p.(=)


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