Variant #0000332636 (NC_000009.11:g.71395246_71395259del, NM_138333.3:c.166_179del (FAM122A))

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.71395246_71395259del
DNA change (hg38) g.68780330_68780343del
Published as FAM122A(NM_138333.3):c.161_174del (p.(Pro56GlufsTer65))
ISCN -
DB-ID FAM122A_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_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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PIP5K1B NM_003558.2 ?/. - c.-86+37673_-86+37686del r.(=) p.(=)
FAM122A NM_138333.3 ?/. - c.166_179del r.(?) p.(Pro56GlufsTer65)


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