Variant #0000307901 (NC_000014.8:g.94849201C>T, NM_001127701.1:c.374G>A (SERPINA1))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.94849201C>T
DNA change (hg38) g.94382864C>T
Published as SERPINA1(NM_000295.4):c.374G>A (p.R125H), SERPINA1(NM_001127701.2):c.374G>A (p.R125H)
ISCN -
DB-ID SERPINA1_000003 See all 35 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) 0.16021 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SERPINA1 NM_001127701.1 -/. - c.374G>A r.(?) p.(Arg125His)


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