Variant #0000552498 (NC_000014.8:g.31358807A>G, NC_000014.8(NM_004086.2):c.1478-15A>G (COCH))

Chromosome 14
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.31358807A>G
DNA change (hg38) g.30889601A>G
Published as -
ISCN -
DB-ID AP4S1_000012
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
AP4S1 NM_001128126.2 ?/. - c.-136258A>G r.(?) p.(=)
COCH NM_004086.2 ?/. - c.1478-15A>G r.(=) p.(=)
STRN3 NM_014574.3 ?/. - c.*5810T>C r.(=) p.(=)


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