Allele/Variant

rs373906087

Species

Homo sapiens

Symbol

rs373906087

Category

Variant

Variant type

SNP

Overlaps

CD164

Location

6:109376105

Nucleotide Change

C>T

Most Severe Consequence

synonymous variant

See all consequences

HGVS.g name

(GRCh38)6:109376105C>T

HGVS.c name

ENSEMBL:ENST00000275080.11:c.331+1795G>A
ENSEMBL:ENST00000310786.10:c.339G>A

HGVS.p name

ENSP00000309376:p.Thr113=
ENSP00000314177:p.Thr113=

Synonyms

Not Available

Notes

Not Available

Cross references

Not Available

References

Not Available

Genome location

Chr6:109366514...109382467 (15.95 kb)

Assembly version

Not Available

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Data currently unavailable; sequence viewer under construction

Variant Molecular Consequences

Sequence feature

Sequence feature type

Associated gene

Location

Molecular consequence

Codon and amino acid change

ENSEMBL:ENST00000275080.11

protein_coding

Intron 3/4

intron variant

ENSEMBL:ENST00000310786.10

protein_coding

Exon 4/6

synonymous variant

337	acG	N/A
[113]	T	N/A

acA

ENSEMBL:ENST00000324953.9

protein_coding

Exon 4/5

synonymous variant

337	acG	N/A
[113]	T	N/A

acA

ENSEMBL:ENST00000413644.6

protein_coding

Exon 4/7

synonymous variant

337	acG	N/A
[113]	T	N/A

acA

ENSEMBL:ENST00000499860.6

transcript

Exon 3/5

non coding transcript exon variant

ENSEMBL:ENST00000504373.2

protein_coding

Exon 4/6

synonymous variant

235	acG	N/A
[79]	T	N/A

acA

ENSEMBL:ENST00000506649.5

transcript

Exon 4/6

non coding transcript exon variant

ENSEMBL:ENST00000512212.1

transcript

Exon 4/4

non coding transcript exon variant

ENSEMBL:ENST00000512821.5

protein_coding

Exon 4/6

synonymous variant

337	acG	N/A
[113]	T	N/A

acA

RefSeq:NM_001142401.3

protein_coding

Intron 3/4

intron variant

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