Variant #0000263207 (NC_000016.9:g.81069612G>T, NM_015251.2:c.137G>T (ATMIN))

Chromosome 16
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.81069612G>T
DNA change (hg38) g.81036007G>T
Published as ATMIN(NM_015251.3):c.137G>T (p.G46V)
ISCN -
DB-ID ATMIN_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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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     
ATMIN NM_015251.2 ?/. - c.137G>T r.(?) p.(Gly46Val)
CMC2 NM_020188.3 ?/. - c.-29309C>A r.(?) p.(=)


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