Variant #0000679139 (NC_000011.9:g.2185527C>T, NM_000207.2:c.-3147G>A (INS))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2185527C>T
DNA change (hg38) -
Published as TH(NM_199292.2):c.1523G>A (p.R508H)
ISCN -
DB-ID IGF2_000067
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.-3147G>A - r.(?) p.(=)
TH NM_000360.3 -?/. - c.1430G>A - r.(?) p.(Arg477His)
IGF2 NM_000612.4 -?/. - c.-26075G>A - r.(?) p.(=)
INS-IGF2 NM_001042376.2 -?/. - c.-3147G>A - r.(?) p.(=)
TH NM_199292.2 -?/. - c.1523G>A - r.(?) p.(Arg508His)


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