Variant #0000655704 (NC_000007.13:g.107566728A>G, NM_002291.2:c.4964T>C (LAMB1))

Chromosome 7
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.107566728A>G
DNA change (hg38) g.107926283A>G
Published as LAMB1(NM_002291.2):c.4964T>C (p.V1655A), LAMB1(NM_002291.3):c.4964T>C (p.V1655A)
ISCN -
DB-ID LAMB1_000036 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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LAMB1 NM_002291.2 ?/. - c.4964T>C r.(?) p.(Val1655Ala)


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