View genomic variant #0000019561

Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
Type -
DNA change (genomic) (Relative to hg19 / GRCh37) g.211540486A>C
Published as -
GERP -
Segregation -
DB-ID CPS1_000006 See all 2 reported entries
MSCV MSCV_0000862
dbSNP ID -
Frequency -
Sources ; clinvar;
Reference -
Variant remarks -
Genetic origin -
Variant_disease -
Average frequency (large NGS studies) Variant not found in online data sets
Owner LOVD




Variant on transcripts

3 entries on 1 page. Showing entries 1 - 3.
Legend  

Gene     

Transcript ID     

AscendingTranscript     

Variant ID     

Affects function     

Location     

Exon     

DNA change (cDNA)     

Protein     

PolyPhen     

GVS function     

Splice distance     

SIFT     
CPS1 00000657 NM_001122633.2 0000019561 ./. - - c.4214A>C p.(Asn1405Thr) - - - -
CPS1 00000659 NM_001122634.2 0000019561 ./. - - c.2843A>C p.(Asn948Thr) - - - -
CPS1 00000658 NM_001875.4 0000019561 ./. - - c.4196A>C p.(Asn1399Thr) - - - -
Legend  


MSeqDR View Variant at Gbrowse

Mitomap Mitochondrial Variant Phenotype Information:

None

Ensembl Variant Phenotype Information:

None