Variant #0000325280 (NC_000017.10:g.18233902A>G, NM_004169.3:c.1138T>C (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.18233902A>G
DNA change (hg38) g.18330588A>G
Published as SHMT1(NM_004169.3):c.1138T>C (p.(Cys380Arg))
ISCN -
DB-ID SHMT1_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SHMT1 NM_004169.3 ?/. - c.1138T>C r.(?) p.(Cys380Arg)
SMCR8 NM_144775.2 ?/. - c.*7518A>G r.(=) p.(=)


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