Variant #0000805942 (NC_000012.11:g.76741323A>G, NM_024685.3:c.442T>C (BBS10))

Chromosome 12
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.76741323A>G
DNA change (hg38) -
Published as BBS10(NM_024685.4):c.442T>C (p.Y148H)
ISCN -
DB-ID BBS10_000135
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OSBPL8 NM_020841.4 ?/. - c.*8346T>C r.(=) p.(=)
BBS10 NM_024685.3 ?/. - c.442T>C r.(?) p.(Tyr148His)


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