Variant #0001053593 (NC_000010.10:g.74928099T>G, NM_173348.1:c.2T>G (FAM149B1))

Chromosome 10
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.74928099T>G
DNA change (hg38) -
Published as FAM149B1(NM_173348.2):c.2T>G (p.(Met1?))
ISCN -
DB-ID ECD_000005 See all 2 reported entries
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) 0.00069 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 2025-11-01 13:22:20 +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     
ECD NM_007265.2 ?/. - c.-489A>C r.(?) p.(=)
FAM149B1 NM_173348.1 ?/. - c.2T>G r.(?) p.?


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