Variant #0000764162 (NC_000023.10:g.100662884A>G, NM_000169.2:c.8T>C (GLA))

Chromosome X
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.100662884A>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID HNRNPH2_000034 See all 4 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs150547672
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0002 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-04-17 11:49:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GLA NM_000169.2 -?/. - c.8T>C r.(?) p.(Leu3Pro)


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