Variant #0000949134 (NC_000009.11:g.103054849C>T, NM_014425.3:c.2310C>T (INVS))

Chromosome 9
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.103054849C>T
DNA change (hg38) -
Published as INVS(NM_014425.4):c.2310C>T (p.H770=), INVS(NM_014425.5):c.2310C>T (p.H770=)
ISCN -
DB-ID INVS_000021 See all 3 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) 0.00084 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INVS NM_014425.3 -?/. - c.2310C>T r.(?) p.(His770=)
TEX10 NM_017746.3 -?/. - c.*9624G>A r.(=) p.(=)


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