Variant #0000332614 (NC_000009.11:g.35107673C>T, NM_013442.1:c.-4582G>A (STOML2))

Chromosome 9
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.35107673C>T
DNA change (hg38) g.35107676C>T
Published as FAM214B(NM_025182.2):c.599G>A (p.(Ser200Asn))
ISCN -
DB-ID FAM214B_000002
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) 0.00019 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
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     
STOML2 NM_013442.1 ?/. - c.-4582G>A r.(?) p.(=)
FAM214B NM_025182.2 ?/. - c.599G>A r.(?) p.(Ser200Asn)


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