Variant #0000503822 (NC_000001.10:g.156830948C>T, NC_000001.10(NM_002529.3):c.212+10C>T (NTRK1))

Chromosome 1
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.156830948C>T
DNA change (hg38) g.156861156C>T
Published as NTRK1(NM_002529.3):c.212+10C>T, NTRK1(NM_002529.4):c.212+10C>T
ISCN -
DB-ID NTRK1_000180 See all 2 reported entries
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) 0.00114 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NTRK1 NM_002529.3 -?/. - c.212+10C>T r.(=) p.(=)
SH2D2A NM_003975.3 -?/. - c.-44448G>A r.(?) p.(=)
INSRR NM_014215.2 -?/. - c.-2535G>A r.(?) p.(=)


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