Variant #0000316740 (NC_000001.10:g.25669518C>T, NM_016124.3:c.*14103C>T (RHD))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.25669518C>T
DNA change (hg38) g.25343027C>T
Published as TMEM50A(NM_014313.4):c.160C>T (p.H54Y)
ISCN -
DB-ID TMEM50A_000001
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 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TMEM50A NM_014313.3 ?/. - c.160C>T r.(?) p.(His54Tyr)
RHD NM_016124.3 ?/. - c.*14103C>T r.(=) p.(=)
C1orf63 NM_020317.3 ?/. - c.-95785G>A r.(?) p.(=)
RHCE NM_020485.4 ?/. - c.*19500G>A r.(=) p.(=)


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