48988708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125578848-T-C

48988758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125578900-T-C

48989286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125579404-T-A

48989286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125579404-T-G

48989739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125579843-G-A

48989739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125579843-G-T

48989940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125580051-G-A

48990123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125580218-T-G

48990336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125580425-A-G

48990448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125580524-T-C

48990803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125580862-T-C

http://identifiers.org/hco/15/GRCh38#48991040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125581072-C-A

http://identifiers.org/hco/15/GRCh38#48991240-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125581256-A-C

48991558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125581546-G-T

48991667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125581636-G-T

48991790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125581749-A-G

http://identifiers.org/hco/15/GRCh38#48991984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125581930-C-A

48991984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125581930-C-G

48992012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125581961-T-C

48992074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125582022-C-G

48992074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 125582022-C-T

http://identifiers.org/hco/15/GRCh38#48992205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125582150-C-A

48992341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, missense_variant
orthologous variants: 125582261-G-A

48992367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582287-T-C

48992367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582287-T-G

48992418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582338-A-G

48992553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582473-C-T

http://identifiers.org/hco/15/GRCh38#48992565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125582482-A-C

48992565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582482-A-G

48992571-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, missense_variant
orthologous variants: 125582488-A-T

48992706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582623-T-A

48992706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125582623-T-C

http://identifiers.org/hco/15/GRCh38#48992850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125582761-C-A

48992895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: synonymous variant
orthologous variants: 125582806-T-C

48992895-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: synonymous variant
orthologous variants: 125582806-T-G

48992913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: synonymous variant
orthologous variants: 125582824-T-C

http://identifiers.org/hco/15/GRCh38#48993048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125583067-C-A

http://identifiers.org/hco/15/GRCh38#48993285-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125583267-A-C

48993672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125583637-A-G

48996301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125585671-T-C

http://identifiers.org/hco/15/GRCh38#48996314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125585684-C-A

48996314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125585684-C-T

48996501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense variant
orthologous variants: 125585868-G-C

48996690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125586017-T-C

http://identifiers.org/hco/15/GRCh38#48996707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125586034-C-A

48996961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125586248-T-C

48996977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125586280-T-C

http://identifiers.org/hco/15/GRCh38#48997115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125586487-C-A

49000007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125587896-C-T

49000185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125588039-T-C

49000768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589204-T-C

49000791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589228-G-A

49000791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589228-G-T

49000947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125589375-G-A

49000947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125589375-G-C

49001129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589558-T-A

49001129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589558-T-C

49001230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125589653-T-C

49008432-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125591353-T-G

49008607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125591526-C-T

http://identifiers.org/hco/15/GRCh38#49008971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125591973-A-C

http://identifiers.org/hco/15/GRCh38#49009071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125592066-C-A

49009071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592066-C-T

49009090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592082-G-A

49009090-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592082-G-C

49009090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592082-G-T

49009094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592086-G-A

49009094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592086-G-T

49009164-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592149-T-A

49009164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592149-T-C

49009175-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592157-T-A

49009376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 125592359-T-C

49009427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592410-G-A

49009549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592527-T-A

49009577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592554-T-C

49010428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125592880-C-T

http://identifiers.org/hco/15/GRCh38#49010434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125592886-A-C

49011140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125593203-T-C

49011449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125593451-A-G

49011491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125593494-A-G

49011501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125593504-G-A

49011501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125593504-G-T

http://identifiers.org/hco/15/GRCh38#49011528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593531-C-A

http://identifiers.org/hco/15/GRCh38#49011631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593612-C-A

49011631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125593612-C-T

49011632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125593613-A-G

49011632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125593613-A-T

http://identifiers.org/hco/15/GRCh38#49011780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593698-C-A

49011780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125593698-C-T

http://identifiers.org/hco/15/GRCh38#49011831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593749-C-A

49011831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125593749-C-T

http://identifiers.org/hco/15/GRCh38#49011970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593874-C-A

49011970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125593874-C-T

http://identifiers.org/hco/15/GRCh38#49011997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125593910-A-C

http://identifiers.org/hco/15/GRCh38#49012220-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125594140-A-C

49012255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594171-G-A

49012272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594188-T-C

49012329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594254-G-A

49012384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594499-T-C

49012446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594557-C-T

49012447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594558-A-G

49012530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594628-G-T

49012533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594631-T-C

49012533-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594631-T-G

49012631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125594717-A-G

49012869-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125594951-T-G

http://identifiers.org/hco/15/GRCh38#49012931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125595022-A-C

49012931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125595022-A-G

49012963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125595040-G-A

49012963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125595040-G-C

49015161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125598386-T-C

49015402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125598526-T-C

49015403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125598527-T-G

49015576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125598654-T-C

49016639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125599193-G-T

49017143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599625-A-G

http://identifiers.org/hco/15/GRCh38#49017159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125599640-C-A

49017159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599640-C-G

49017159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599640-C-T

49017178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599659-T-A

49017432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599884-C-T

49017447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125599921-C-T

49017493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125600029-T-C

49017644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125600183-T-C

49017703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125600512-G-A

49017703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125600512-G-T

49017712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125600521-G-A

49017712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 125600521-G-T

49019584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125602340-A-G

49019587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125602343-T-C

49019622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125602376-A-G

http://identifiers.org/hco/15/GRCh38#49019641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125602395-C-A

49019641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125602395-C-T

49021054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125603227-C-T

49021490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125603628-T-A

49021638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125603758-C-G

49021638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125603758-C-T

49024840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125606068-T-C

49026831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125607054-G-T

49026850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125607073-A-G

49026856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125607079-T-C

49027470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: synonymous variant
orthologous variants: 125609400-A-G

49027475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: missense variant
orthologous variants: 125609405-C-T

http://identifiers.org/hco/15/GRCh38#49027601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125609509-A-C

49027601-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125609509-A-T

49028083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -G-A

49028083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -G-C

49028083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -G-T

49028112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -T-C

http://identifiers.org/hco/15/GRCh38#49028215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125609803-C-A

49028215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125609803-C-T

49028224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -C-G

49028224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: -C-T

49028297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125609853-T-C

49028297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125609853-T-G

49028376-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125609942-T-A

49028538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, missense_variant
orthologous variants: 125610109-C-T

49028591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125610162-G-A

49028611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, missense_variant
orthologous variants: 125610182-T-C

49028819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125610369-G-A

49028819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125610369-G-C

49028819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125610369-G-T

http://identifiers.org/hco/15/GRCh38#49032954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125613318-C-A

http://identifiers.org/hco/15/GRCh38#49033013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125613377-C-A

49033114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613484-A-G

49033134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613504-A-T

49033148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613526-T-C

49033149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613527-G-A

49033149-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613527-G-C

49033149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613527-G-T

49033162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613537-T-A

49033162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125613537-T-C

49033979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125614160-T-C

http://identifiers.org/hco/15/GRCh38#49034022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125614203-C-A

49034087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125614266-G-T

http://identifiers.org/hco/15/GRCh38#49034102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125614281-C-A

49034102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125614281-C-G

49035299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125615058-T-A

49035299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125615058-T-C

49035431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 125615193-G-A

49035544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 125615306-A-G

49036652-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron variant
orthologous variants: 125616328-G-C

49037209-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, undefined
orthologous variants: 125616968-T-G

http://identifiers.org/hco/15/GRCh38#49037559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125617448-C-A

49037559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 125617448-C-T

49037617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125617499-T-C

49037617-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125617499-T-G

49037736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 125617618-T-C

49037740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 125617622-T-C

49037886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125617728-A-G

http://identifiers.org/hco/15/GRCh38#49037912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125617751-C-A

49038029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125617856-A-T

49038168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125617984-A-G

http://identifiers.org/hco/15/GRCh38#49040388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125619154-C-A

49040388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125619154-C-T

49040929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125619314-T-C

49041513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620396-T-C

http://identifiers.org/hco/15/GRCh38#49041550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125620435-C-A

49041563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620447-G-A

49041563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620447-G-T

49041582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620466-T-G

49041706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620584-T-A

49042154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125620954-G-C

49042221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125621026-T-C

http://identifiers.org/hco/15/GRCh38#49042308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125621112-C-A

49042310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125621114-T-C

49042649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125621180-A-G

49042665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125621192-G-A

49042666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125621193-T-C

49043784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125622754-T-C

49043881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125622836-C-G

49044000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125622935-G-A

49044541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125623183-T-C

http://identifiers.org/hco/15/GRCh38#49044659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125623282-A-C

49044659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125623282-A-T

49044797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125623410-C-T

49044889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125623496-T-C

49045038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 125623634-G-A

http://identifiers.org/hco/15/GRCh38#49045723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#125624340-A-C

http://identifiers.org/hco/15/GRCh38#49046416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#125624648-C-A

49046416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28997
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 125624648-C-T