Variant #0001066874 (NC_000017.10:g.71239110T>C, NM_032837.2:c.-10665A>G (FAM104A))

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.71239110T>C
DNA change (hg38) -
Published as C17orf80(NM_001351264.2):c.1697T>C (p.(Val566Ala))
ISCN -
DB-ID C17orf80_000002
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) 0.00017 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 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CPSF4L NM_001129885.1 ?/. - c.*5523A>G r.(=) p.(=)
C17orf80 NM_017941.4 ?/. - c.1697T>C r.(?) p.(Val566Ala)
FAM104A NM_032837.2 ?/. - c.-10665A>G r.(?) p.(=)


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