Variant #0000316584 (NC_000011.9:g.2186478C>A, NM_000207.2:c.-4098G>T (INS))

Chromosome 11
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.2186478C>A
DNA change (hg38) g.2165248C>A
Published as TH(NM_199292.2):c.1411G>T (p.A471S)
ISCN -
DB-ID TH_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) 9.0E-5 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 ?/. - c.-4098G>T - r.(?) p.(=)
TH NM_000360.3 ?/. - c.1318G>T - r.(?) p.(Ala440Ser)
IGF2 NM_000612.4 ?/. - c.-27026G>T - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.-4098G>T - r.(?) p.(=)
TH NM_199292.2 ?/. - c.1411G>T - r.(?) p.(Ala471Ser)


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