Variant #0000855074 (NC_000017.10:g.66364750G>A, NM_001267727.1:c.766G>A (ARSG))

Chromosome 17
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.66364750G>A
DNA change (hg38) -
Published as ARSG(NM_001352910.1):c.766G>A (p.V256M)
ISCN -
DB-ID SLC16A6_000014
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) 0.00036 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 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARSG NM_001267727.1 ?/. - c.766G>A r.(?) p.(Val256Met)
SLC16A6 NM_004694.4 ?/. - c.-77531C>T r.(?) p.(=)
ARSG NM_014960.4 ?/. - c.766G>A r.(?) p.(Val256Met)
WIPI1 NM_017983.5 ?/. - c.*53164C>T r.(=) p.(=)


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