131574011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802555-T-A

131574011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802555-T-C

131574039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802540-A-G

131574045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802534-G-T

131574075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802497-G-C

131574075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802497-G-T

131574129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802443-T-A

131574141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802434-T-C

131574187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802392-A-G

131574220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802350-T-C

131574266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802308-G-A

131574306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802245-A-G

131574423-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24802128-A-T

131574563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24801353-T-C

131574563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24801353-T-G

131574833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24801094-T-C

131574853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24801075-G-T

131574994-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800965-A-T

131574996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800963-T-C

131575007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800952-T-C

131575039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800917-A-T

131575064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800891-G-C

http://identifiers.org/hco/6/GRCh38#131575079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24800876-C-A

131575079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800876-C-G

131575094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24800860-A-G

131575470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799673-A-G

131575496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799649-G-C

131575527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799618-G-T

http://identifiers.org/hco/6/GRCh38#131575556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24799589-C-A

131575556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799589-C-T

131575642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799504-G-A

131576028-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24799135-T-A

131576228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798949-G-A

131576324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798915-T-C

131576534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798713-T-C

131576582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798664-T-G

131576640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798613-T-C

http://identifiers.org/hco/6/GRCh38#131577079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24798210-C-A

131577090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798198-G-T

131577135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798154-C-T

131577136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798153-C-T

131577171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798137-T-C

131577264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24798112-G-T

131577572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24797934-T-C

131577803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24797725-G-A

131578025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24797551-T-C

131578323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24797394-C-T

http://identifiers.org/hco/6/GRCh38#131578324-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24797393-A-C

131578800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796878-C-G

131579089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 24796714-A-G

131579163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 24796641-C-T

131579301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24796504-T-C

http://identifiers.org/hco/6/GRCh38#131579618-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24795672-A-C

131580179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794881-T-C

131580351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794725-G-A

131580411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794677-A-G

http://identifiers.org/hco/6/GRCh38#131580415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24794673-C-A

131580471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794619-T-C

131580573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794582-G-A

131580664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794479-C-T

131581106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794080-A-G

http://identifiers.org/hco/6/GRCh38#131581123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24794068-C-A

131581142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24794049-G-T

131581390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793797-G-A

131581390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793797-G-T

131581396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793791-A-T

http://identifiers.org/hco/6/GRCh38#131581399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24793788-C-A

131581399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793788-C-G

131581399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793788-C-T

131581419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793768-T-C

131581425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793763-G-C

131581425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793763-G-T

http://identifiers.org/hco/6/GRCh38#131581431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24793757-C-A

131581431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793757-C-T

131581445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793743-G-A

131581445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793743-G-T

131581494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793693-T-G

131581699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793207-T-C

131581746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793163-C-T

131581781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793128-T-C

131581791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24793117-A-G

131582687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24792699-G-T

131582725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792661-T-C

131582843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792538-A-G

http://identifiers.org/hco/6/GRCh38#131582991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24792424-C-A

http://identifiers.org/hco/6/GRCh38#131582992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24792423-C-A

131582992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792423-C-T

131583004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792411-A-G

131583033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792384-A-G

131583335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24792080-C-T

131583389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24792026-G-A

131583389-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24792026-G-C

http://identifiers.org/hco/6/GRCh38#131583574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24791841-C-A

http://identifiers.org/hco/6/GRCh38#131583579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24791838-C-A

131583579-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791838-C-G

131583579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791838-C-T

131583628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791793-T-C

131583635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791786-T-C

131583654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791770-G-A

131583654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24791770-G-T

http://identifiers.org/hco/6/GRCh38#131583778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24791639-C-A

131583778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24791639-C-T

131583786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24791631-G-T

131583798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24791619-G-A

131583846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24791571-T-G

http://identifiers.org/hco/6/GRCh38#131584024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#24791389-C-A

131584024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24791389-C-T

131584033-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791380-T-A

http://identifiers.org/hco/6/GRCh38#131584037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24791376-C-A

131584037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791376-C-T

131584038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791375-T-C

131584038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791375-T-G

131584046-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791367-T-C

131584046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24791367-T-G

131584332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24791114-A-G

131584354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24791094-A-T

131584389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24791060-C-T

131584616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790892-T-C

131585100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790758-T-A

131585121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790738-G-A

131585123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790736-T-C

131585166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790701-C-T

131585275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790578-C-T

131585325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790528-C-G

131585325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790528-C-T

131585377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790477-C-G

131585805-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790105-G-C

131585807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24790103-C-G

131586042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789873-G-A

131586042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789873-G-T

131586448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789783-A-G

131586466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789766-T-G

131586494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789738-T-C

131586576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24789682-T-G

http://identifiers.org/hco/6/GRCh38#131586608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789650-A-C

http://identifiers.org/hco/6/GRCh38#131586619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789639-C-A

http://identifiers.org/hco/6/GRCh38#131586748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789555-C-A

131586748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789555-C-T

131586760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789543-T-C

131586770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789537-T-C

131586889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789431-G-A

131586889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789431-G-C

131586889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789431-G-T

http://identifiers.org/hco/6/GRCh38#131586897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789423-A-C

131586897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789423-A-T

131587043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789308-T-C

131587043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789308-T-G

http://identifiers.org/hco/6/GRCh38#131587145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789188-C-A

131587145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789188-C-G

131587145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789188-C-T

http://identifiers.org/hco/6/GRCh38#131587167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24789154-C-A

131587167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789154-C-G

131587167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789154-C-T

131587287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789052-G-A

131587295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24789044-T-G

http://identifiers.org/hco/6/GRCh38#131587451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24788901-A-C

131587498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24788856-G-C

131587574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24788800-T-C

131587700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24788702-C-T

131587854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24788551-A-G

http://identifiers.org/hco/6/GRCh38#131587883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24788537-A-C

131587914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788525-G-A

131587914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788525-G-T

http://identifiers.org/hco/6/GRCh38#131587978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24788492-C-A

131587978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24788492-C-T

http://identifiers.org/hco/6/GRCh38#131588193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24788298-A-C

131588538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787915-T-C

131588598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787728-G-C

131588671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787500-A-G

131588860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787323-A-G

131588868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787315-C-T

131589075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787133-G-A

131589109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24787087-G-T

131589324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786892-G-T

131589361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786861-T-C

131589382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786840-C-G

131589382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786840-C-T

http://identifiers.org/hco/6/GRCh38#131589632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24786599-C-A

131589632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786599-C-G

131589651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786580-G-T

131589655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786576-G-C

131589655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786576-G-T

http://identifiers.org/hco/6/GRCh38#131589685-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24786551-A-C

131589721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786518-T-A

131589721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786518-T-C

http://identifiers.org/hco/6/GRCh38#131589732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24786509-C-A

131589732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786509-C-T

131589885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786382-T-C

131589890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786361-C-T

131589898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786353-G-A

131589912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786339-C-T

131589977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24786111-C-T

http://identifiers.org/hco/6/GRCh38#131590152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24785954-C-A

131590152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785954-C-T

131590186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785922-A-T

131590189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785919-T-C

http://identifiers.org/hco/6/GRCh38#131590202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24785906-C-A

131590204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785904-G-T

131590207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785901-A-G

131590299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785832-A-G

http://identifiers.org/hco/6/GRCh38#131590332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24785804-C-A

http://identifiers.org/hco/6/GRCh38#131590371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24785765-C-A

131590371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24785765-C-T

131590419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24785717-G-A

131590444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 24785692-T-C

131590446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24785690-A-G

131590446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24785690-A-T

131590461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785675-A-T

131590464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785672-C-T

131590465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785671-T-C

http://identifiers.org/hco/6/GRCh38#131590472-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24785664-A-C

131590472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785664-A-G

131590477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785652-A-G

131590544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24785594-T-G

131591445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24784611-C-G

131591445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24784611-C-T

131591463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24784593-G-A

131591463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24784593-G-T

131591520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24784536-T-C

http://identifiers.org/hco/6/GRCh38#131591549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24784510-A-C

131591549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784510-A-G

131591583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784473-A-G

131591583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784473-A-T

131591710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784346-G-A

131591710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784346-G-T

131591734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24784315-T-C

131592374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24783917-A-G

131592604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783710-T-C

131592730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783529-G-A

131592730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783529-G-T

http://identifiers.org/hco/6/GRCh38#131592784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24783436-C-A

131592802-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783427-A-T

http://identifiers.org/hco/6/GRCh38#131592831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24783393-C-A

131592847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783377-A-G

131592875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24783350-G-T

131593111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24783138-G-A

131594079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781974-A-G

131594140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24781913-T-C

131594259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24781794-T-G

http://identifiers.org/hco/6/GRCh38#131594400-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24781657-C-A

131594456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781604-A-G

131594467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781593-T-C

131594539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781534-A-G

131594901-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24781207-G-C

131595237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780973-A-G

131595826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24780470-A-T

http://identifiers.org/hco/6/GRCh38#131595827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24780469-A-C

http://identifiers.org/hco/6/GRCh38#131596236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24780000-A-C

131596237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779999-A-T

131596251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779980-T-C

http://identifiers.org/hco/6/GRCh38#131596281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24779930-C-A

http://identifiers.org/hco/6/GRCh38#131596324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24779889-C-A

131596325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779888-T-C

131596325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779888-T-G

http://identifiers.org/hco/6/GRCh38#131596447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24779779-C-A

http://identifiers.org/hco/6/GRCh38#131596448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24779778-C-A

131596452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779774-T-C

131596461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779765-C-G

131596509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779736-G-C

131596509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24779736-G-T

131596834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24779453-G-A

131596834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24779453-G-T

131597081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24779241-C-G

http://identifiers.org/hco/6/GRCh38#131598123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24778524-A-C

131598123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24778524-A-G

131598215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24778442-A-G

131598222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24778435-C-T

http://identifiers.org/hco/6/GRCh38#131598223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24778434-A-C

131598223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24778434-A-G

131598252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, stop_lost
orthologous variants: 24778405-T-G

131598315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, missense_variant
orthologous variants: 24778341-A-G

http://identifiers.org/hco/6/GRCh38#131598462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#24778194-A-C

131598822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777835-G-A

131598822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777835-G-T

131598901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777727-A-G

131598980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777456-T-G

131599097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777339-G-A

131599212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777254-T-A

131599395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777112-T-C

131599423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24777085-T-C

131599667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776919-A-G

131599996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776757-G-T

131600209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776551-C-T

http://identifiers.org/hco/6/GRCh38#131600216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24776544-C-A

131600216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776544-C-T

131600492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776331-T-C

131600675-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776152-T-G

131600677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24776150-T-A

131600827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24775878-C-T

131601409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24775129-A-G

131601562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24774992-T-A

131601763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24774788-T-C

131602123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24774547-A-G

131602132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24774538-T-C

131602277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24774410-T-A

131602277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24774410-T-C

131602948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24773336-G-T

131602952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24773332-A-G

131602991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24773297-T-C

131603022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24773267-G-A

131603022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24773267-G-T

131603066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 24773219-G-A

131603066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 24773219-G-T

131603214-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24773071-A-T

131603221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24773067-A-G

131603291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24772999-A-T

http://identifiers.org/hco/6/GRCh38#131603314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24772978-C-A

131603314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24772978-C-T

http://identifiers.org/hco/6/GRCh38#131603347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24772952-C-A

131603832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24772037-G-A

131603832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24772037-G-T

131603860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24772011-T-C

http://identifiers.org/hco/6/GRCh38#131603892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24771988-C-A

131604077-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771819-G-C

131604077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771819-G-T

131604169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771753-C-T

131604245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 24771677-T-C

131604323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 24771599-G-A

131604523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771409-T-C

131604533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771377-T-C

131604536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771374-G-A

131604730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771156-T-A

131604730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771156-T-G

131604866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24771043-T-C

http://identifiers.org/hco/6/GRCh38#131605156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24769830-C-A

131605156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769830-C-T

http://identifiers.org/hco/6/GRCh38#131605158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24769828-C-A

131605158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769828-C-G

131605158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769828-C-T

http://identifiers.org/hco/6/GRCh38#131605192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24769792-C-A

131605192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769792-C-T

http://identifiers.org/hco/6/GRCh38#131605231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24769765-A-C

131605321-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, missense_variant
orthologous variants: 24769675-C-G

131605330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, missense_variant
orthologous variants: 24769666-G-C

131605351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, missense_variant
orthologous variants: 24769645-C-G

131605590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769423-A-G

131605590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769423-A-T

131605936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769081-T-A

131605936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769081-T-C

131606000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769030-A-G

131606022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769010-T-C

131606024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769008-T-C

131606028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24769004-T-C

131606252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768783-T-A

131606369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768671-G-C

131606369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768671-G-T

131606373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768661-G-A

131606373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768661-G-T

http://identifiers.org/hco/6/GRCh38#131606717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24768330-C-A

131606738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768312-A-G

131606826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768228-A-G

131606978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24768076-T-C

131607404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767782-G-A

131607544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767644-A-G

131607558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767630-A-G

131607559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767629-A-G

131607584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767595-T-C

131607687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767490-T-C

131607777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767401-G-A

131607779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767399-A-G

131607786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767392-G-C

131607786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767392-G-T

131607796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767382-G-A

131607796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767382-G-T

131607822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767358-T-C

131607900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767180-T-C

131607913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24767173-C-T

131608093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24766993-A-G

131608093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24766993-A-T

131609101-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24765771-G-C

131609150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24765733-G-A

131609314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24765584-T-G

http://identifiers.org/hco/6/GRCh38#131609319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24765579-C-A

131609322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24765576-C-G

131609751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764956-T-C

http://identifiers.org/hco/6/GRCh38#131609896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24764824-A-C

131609915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764805-A-G

131609945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764600-G-A

131609945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764600-G-T

131609952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764594-T-A

131609952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764594-T-C

131610016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764527-G-A

131610293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764250-G-C

131610293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764250-G-T

131610381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764166-A-G

131610402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764145-T-C

http://identifiers.org/hco/6/GRCh38#131610465-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24764042-A-C

131610465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24764042-A-G

131610522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24763870-G-C

131611081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24763359-T-C

131611489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24762934-G-T

131611911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24762541-C-T

http://identifiers.org/hco/6/GRCh38#131612089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24762353-C-A

131612089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24762353-C-T

131612100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24762337-C-G

http://identifiers.org/hco/6/GRCh38#131612252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24762203-A-C

131612579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761704-A-T

131612592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761691-T-C

131612697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761589-G-C

131612892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761459-C-T

131613000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761365-A-G

131613088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761297-T-A

131613154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761277-A-G

131613310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24761134-C-T

131613662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24760790-A-G

131613905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24760538-T-C

131614082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24760301-G-A

131614160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24760246-A-G

131614916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24759526-T-C

http://identifiers.org/hco/6/GRCh38#131615230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24759210-C-A

131615230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24759210-C-T

http://identifiers.org/hco/6/GRCh38#131615445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24758996-C-A

131615445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24758996-C-G

131615445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24758996-C-T

131615701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24758745-T-C

131615708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24758738-T-C

http://identifiers.org/hco/6/GRCh38#131616221-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24758245-A-C

131618390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24755697-T-A

131618390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24755697-T-C

131618441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24755647-C-T

131618555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24755533-G-T

131618562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24755526-G-T

http://identifiers.org/hco/6/GRCh38#131619750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24754427-A-C

131619750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24754427-A-G

131619891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: synonymous variant
orthologous variants: 24754290-A-G

http://identifiers.org/hco/6/GRCh38#131619940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24754250-A-C

131619948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24754242-T-C

http://identifiers.org/hco/6/GRCh38#131619983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24754212-A-C

131619998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24754188-A-G

131620193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24753999-C-G

131620641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24752924-T-C

131620644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24752921-C-T

131620761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24752808-G-A

131620761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24752808-G-C

131620761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24752808-G-T

131621727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24752034-A-G

131621761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751940-T-A

131622002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751459-G-C

131622002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751459-G-T

131622147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751323-C-T

131622216-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751266-T-G

131622227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24751255-T-C

131622881-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750985-C-G

131623240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750685-C-T

131623290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750642-T-C

131623290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750642-T-G

131623326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750602-A-G

131623326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750602-A-T

131623430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24750498-G-A

131623430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: missense variant
orthologous variants: 24750498-G-C

131623478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750446-T-C

131623539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750404-G-A

131623539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750404-G-T

http://identifiers.org/hco/6/GRCh38#131624050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24750200-A-C

http://identifiers.org/hco/6/GRCh38#131624072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24750180-A-C

131624223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24750047-C-G

131624470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24749838-T-C

131624526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24749780-G-A

131624526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24749780-G-C

131625053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24749302-T-C

131625730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24748947-G-A

131626568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24747296-T-C

131626640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron variant
orthologous variants: 24747225-C-T

131627001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746991-T-C

131627100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746906-T-C

http://identifiers.org/hco/6/GRCh38#131627134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24746872-C-A

131627134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746872-C-T

131627147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746859-A-G

131627160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746846-T-C

131627181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746829-T-A

131627181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746829-T-G

http://identifiers.org/hco/6/GRCh38#131627202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24746807-C-A

131627202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746807-C-T

131627350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746692-G-A

131627350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746692-G-C

131627350-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746692-G-T

131627390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746653-G-A

131627601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24746421-A-G

http://identifiers.org/hco/6/GRCh38#131627928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24746121-C-A

131627928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24746121-C-G

131627928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24746121-C-T

131627934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24746115-C-T

http://identifiers.org/hco/6/GRCh38#131628050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#24746003-C-A

131628050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24746003-C-T

131628067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24745985-C-T

131628286-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2372
most severe consequence: 5 prime UTR variant
orthologous variants: 24745813-A-G