Variant #0001005145 (NC_000019.9:g.56001766C>T, NM_001144950.1:c.577C>T (SSC5D))

Chromosome 19
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.56001766C>T
DNA change (hg38) -
Published as SSC5D(NM_001144950.1):c.577C>T (p.(Pro193Ser))
ISCN -
DB-ID NAT14_000004
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_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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SSC5D NM_001144950.1 -?/. - c.577C>T r.(?) p.(Pro193Ser)
NAT14 NM_020378.3 -?/. - c.*3443C>T r.(=) p.(=)


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