Variant #0000330857 (NC_000006.11:g.30883798T>G, NM_020442.4:c.547T>G (VARS2))

Chromosome 6
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.30883798T>G
DNA change (hg38) g.30916021T>G
Published as VARS2(NM_001167733.1):c.127T>G (p.(Ser43Ala))
ISCN -
DB-ID VARS2_000009
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) 4.0E-5 View details
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     
GTF2H4 NM_001517.4 ?/. - c.*2038T>G r.(=) p.(=)
VARS2 NM_020442.4 ?/. - c.547T>G r.(?) p.(Ser183Ala)


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