Variant #0001035368 (NC_000005.9:g.94891080A>G, NM_014639.3:c.-668T>C (TTC37))

Chromosome 5
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.94891080A>G
DNA change (hg38) -
Published as ARSK(NM_198150.3):c.98A>G (p.(Asn33Ser))
ISCN -
DB-ID ARSK_000005
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TTC37 NM_014639.3 ?/. - c.-668T>C r.(?) p.(=)
ARSK NM_198150.2 ?/. - c.98A>G r.(?) p.(Asn33Ser)


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