Variant #0000349761 (NC_000012.11:g.57638105C>G, NM_005412.5:c.*9961C>G (SHMT2))

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.57638105C>G
DNA change (hg38) g.57244322C>G
Published as -
ISCN -
DB-ID STAC3_000001 See all 4 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) 9.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
SHMT2 NM_005412.5 ?/. - c.*9961C>G r.(=) p.(=)
NDUFA4L2 NM_020142.3 ?/. - c.-3824G>C r.(?) p.(=)
STAC3 NM_145064.1 ?/. - c.851G>C r.(?) p.(Trp284Ser)


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