Variant #0000256122 (NC_000007.13:g.41739713A>C, NM_002192.2:c.260T>G (INHBA))

Chromosome 7
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.41739713A>C
DNA change (hg38) g.41700115A>C
Published as INHBA(NM_002192.4):c.260T>G (p.I87S)
ISCN -
DB-ID INHBA_000003
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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INHBA NM_002192.2 ?/. - c.260T>G r.(?) p.(Ile87Ser)
INHBA-AS1 NR_027118.1 ?/. - n.173+6027A>C r.(?) -


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