Variant #0000807852 (NC_000017.10:g.18233949C>T, NM_004169.3:c.1091G>A (SHMT1))

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.18233949C>T
DNA change (hg38) -
Published as SHMT1(NM_004169.4):c.1091G>A (p.R364H)
ISCN -
DB-ID SHMT1_000005
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) 0.00016 View details
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHMT1 NM_004169.3 ?/. - c.1091G>A r.(?) p.(Arg364His)
SMCR8 NM_144775.2 ?/. - c.*7565C>T r.(=) p.(=)


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