Variant #0000316582 (NC_000011.9:g.2186928G>C, INS(NM_000207.2):c.-4548C>G)

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.2186928G>C
DNA change (hg38) g.2165698G>C
Published as TH(NM_199292.2):c.1263C>G (p.A421=)
ISCN -
DB-ID TH_000012
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) 0.00024 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
INS NM_000207.2 ?/. - c.-4548C>G - r.(?) p.(=)
TH NM_000360.3 ?/. - c.1170C>G - r.(?) p.(Ala390=)
IGF2 NM_000612.4 ?/. - c.-27476C>G - r.(?) p.(=)
INS-IGF2 NM_001042376.2 ?/. - c.-4548C>G - r.(?) p.(=)
TH NM_199292.2 ?/. - c.1263C>G - r.(?) p.(Ala421=)