Variant #0000325999 (NC_000019.9:g.460729G>A, NM_012435.2:c.268C>T (SHC2))

Chromosome 19
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.460729G>A
DNA change (hg38) g.460729G>A
Published as SHC2(NM_012435.2):c.268C>T (p.(Pro90Ser))
ISCN -
DB-ID SHC2_000004
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     
SHC2 NM_012435.2 ?/. - c.268C>T r.(?) p.(Pro90Ser)
ODF3L2 NM_182577.2 ?/. - c.*3115C>T r.(=) p.(=)


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