Variant #0000571750 (NC_000022.10:g.30735213T>C, NM_001017437.2:c.-18074T>C (CCDC157))

Chromosome 22
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.30735213T>C
DNA change (hg38) g.30339224T>C
Published as SF3A1(NM_001005409.1):c.1208A>G (p.(Gln403Arg))
ISCN -
DB-ID CCDC157_000003
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 2019-07-18 18:22:55 +02:00 (CEST)
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     
CCDC157 NM_001017437.2 ?/. - c.-18074T>C r.(?) p.(=)
SF3A1 NM_005877.4 ?/. - c.1403A>G r.(?) p.(Gln468Arg)


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