Variant #0000721319 (NC_000007.13:g.142983735G>A, NM_032982.3:c.-1814G>A (CASP2))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.142983735G>A
DNA change (hg38) -
Published as TMEM139(NM_001282876.2):c.464G>A (p.S155N)
ISCN -
DB-ID TMEM139_000001 See all 2 reported entries
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) 0.00103 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-11-25 20:51:44 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CASP2 NM_032982.3 -?/. - c.-1814G>A r.(?) p.(=)
TMEM139 NM_153345.2 -?/. - c.464G>A r.(?) p.(Ser155Asn)


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