Variant #0000722208 (NC_000009.11:g.111929287T>G, NM_014334.2:c.285A>C (FRRS1L))

Chromosome 9
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.111929287T>G
DNA change (hg38) -
Published as FRRS1L(NM_014334.3):c.285A>C (p.G95=)
ISCN -
DB-ID EPB41L4B_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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FRRS1L NM_014334.2 ?/. - c.285A>C r.(?) p.(Gly95=)
EPB41L4B NM_018424.2 ?/. - c.*74655A>C r.(=) p.(=)


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