Variant #0001040302 (NC_000015.9:g.38776752_38776769del, NM_005739.3:c.*6004_*6021del (RASGRP1))

Chromosome 15
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.38776752_38776769del
DNA change (hg38) -
Published as FAM98B(NM_173611.4):c.1194_1211del (p.(Gly404_Gly409del))
ISCN -
DB-ID FAM98B_000004
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_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     
RASGRP1 NM_005739.3 ?/. - c.*6004_*6021del r.(=) p.(=)
FAM98B NM_173611.2 ?/. - c.1194_1211del r.(?) p.(Gly404_Gly409del)


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