Variant #0000274535 (NC_000018.9:g.77440160G>C, NM_004715.4:c.213G>C (CTDP1))

Chromosome 18
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.77440160G>C
DNA change (hg38) g.79680160G>C
Published as CTDP1(NM_001318511.2):c.213G>C (p.G71=), CTDP1(NM_004715.4):c.213G>C (p.G71=), CTDP1(NM_004715.5):c.213G>C (p.G71=), CTDP1(NM_048368.4):c.213G>C ...)
ISCN -
DB-ID CTDP1_000005 See all 2 reported entries
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CTDP1 NM_004715.4 -?/. - c.213G>C r.(?) p.(Gly71=)


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