http://identifiers.org/hco/6/GRCh38#42564076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47321399-C-A

42564076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5 prime UTR variant
orthologous variants: 47321399-C-T

42564185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47321291-T-G

42564199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47321276-G-A

42564199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47321276-G-T

http://identifiers.org/hco/6/GRCh38#42564203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47321272-C-A

42564203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47321272-C-G

42564281-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 47321194-T-A

42564383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense_variant, undefined
orthologous variants: 47321080-G-C

42564433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant
orthologous variants: 47321029-T-C

http://identifiers.org/hco/6/GRCh38#42564475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47320987-C-A

http://identifiers.org/hco/6/GRCh38#42564524-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47320942-C-A

42564524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 47320942-C-T

42564745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47320757-C-T

42564764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47320738-A-T

http://identifiers.org/hco/6/GRCh38#42564900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47320601-A-C

42564900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47320601-A-G

42565374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47320052-T-A

42565927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47319835-T-A

42566110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47319641-T-C

42566205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47319567-G-T

42569013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47317365-A-T

42569021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47317357-A-G

42569237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47317149-A-G

42569651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47316869-T-A

42569772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47316755-A-G

42571762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47314631-T-G

42571961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47314220-T-C

42572152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, undefined
orthologous variants: 47314098-A-T

42572242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47314022-C-G

42573444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47312058-T-C

42573595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311923-G-A

42573595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311923-G-C

42573595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311923-G-T

42573633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311869-G-A

http://identifiers.org/hco/6/GRCh38#42573683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47311819-A-C

42573683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311819-A-G

42573705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311791-A-G

42573723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311780-T-C

42573726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47311777-T-C

42573749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47311754-A-G

http://identifiers.org/hco/6/GRCh38#42573757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47311746-C-A

42573757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: synonymous variant
orthologous variants: 47311746-C-T

http://identifiers.org/hco/6/GRCh38#42574314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47311268-A-C

42574329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311253-T-G

42574378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311218-A-G

42574514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311087-A-G

42574597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311022-G-A

42574600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47311019-G-C

http://identifiers.org/hco/6/GRCh38#42575415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47310237-A-C

42575786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309909-C-T

42575806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309893-C-G

42575973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309727-G-A

42576130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309564-T-C

42576274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309414-A-G

42576320-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309376-G-C

42576420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309309-G-T

42576439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47309290-T-C

42592133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47304011-T-C

42592200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47303944-G-A

42592256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47303888-G-A

42592709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47303068-T-C

42593435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302667-T-G

http://identifiers.org/hco/6/GRCh38#42593466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47302637-C-A

42593536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302539-T-C

42593732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302364-A-G

http://identifiers.org/hco/6/GRCh38#42593970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47302219-A-C

42594084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302130-T-A

42594093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302121-A-T

http://identifiers.org/hco/6/GRCh38#42594147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47302070-C-A

42594147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302070-C-T

42594176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47302045-C-T

42594197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47302023-A-G

42594200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47302020-T-A

http://identifiers.org/hco/6/GRCh38#42594278-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47301942-A-C

42594327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47301896-G-A

42603263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299999-A-G

42603269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299993-T-C

42603660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47299635-G-A

42603745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299554-G-A

http://identifiers.org/hco/6/GRCh38#42603794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47299504-A-C

42603794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299504-A-G

http://identifiers.org/hco/6/GRCh38#42603822-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47299278-A-C

42603822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299278-A-G

42603869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47299232-T-C

42604095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47298940-T-A

42606360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297211-G-A

http://identifiers.org/hco/6/GRCh38#42606460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47297098-A-C

42606460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297098-A-G

42606461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297097-G-A

42606462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297096-G-A

42606462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297096-G-T

42606467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297091-G-A

42606470-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297088-T-A

42606470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297088-T-C

42606484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47297075-A-G

42606573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296991-T-A

42606573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296991-T-C

http://identifiers.org/hco/6/GRCh38#42606735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47296828-C-A

42606735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296828-C-T

42606765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296803-G-A

42606765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296803-G-C

42606765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47296803-G-T

42612024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294373-G-A

42612024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294373-G-T

42612105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294329-T-G

42612108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294326-C-T

42612124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294311-G-A

42612160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294276-T-C

42612160-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47294276-T-G

42612207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: stop gained
orthologous variants: 47294229-C-T

42614632-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293727-A-G

42614983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293384-T-G

http://identifiers.org/hco/6/GRCh38#42614986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47293380-A-C

42614986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293380-A-G

http://identifiers.org/hco/6/GRCh38#42615004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47293359-C-A

42615256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293135-G-A

42615256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293135-G-C

42615256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293135-G-T

42615272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293119-T-C

42615284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47293107-T-C

42616130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47292224-A-G

42616174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47292188-T-A

42616337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47292045-A-G

42616880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291764-G-C

42616887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291757-C-T

42616897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291749-G-A

http://identifiers.org/hco/6/GRCh38#42617139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47291585-C-A

42617139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291585-C-T

http://identifiers.org/hco/6/GRCh38#42617156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47291572-C-A

42617225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291526-C-T

42617285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, stop_gained
orthologous variants: 47291466-C-T

42617303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant
orthologous variants: 47291448-G-A

42617303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant
orthologous variants: 47291448-G-T

42617348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291403-G-T

42617360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291391-T-C

42617375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291376-T-C

42617598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291172-A-G

42617645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291125-A-G

42617697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291083-A-G

42617810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47291014-A-G

42628103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288330-G-A

42628265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288230-T-C

http://identifiers.org/hco/6/GRCh38#42628316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47288189-C-A

42628333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288172-T-C

42628360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288138-A-G

http://identifiers.org/hco/6/GRCh38#42628362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47288136-A-C

42628362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288136-A-G

42628446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47288044-G-A

42631746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287608-T-C

42631872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287524-A-T

http://identifiers.org/hco/6/GRCh38#42631920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47287500-A-C

42631920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287500-A-G

42631920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287500-A-T

42631922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287498-A-T

42631942-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287490-T-A

42631942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287490-T-G

42632184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287322-G-C

42632421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287121-G-T

42632435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287107-T-C

42632435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287107-T-G

42632477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287065-G-A

42632477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287065-G-T

42632533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47287032-T-C

42632552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 47287014-G-T

42632562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47287004-T-C

42632562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47287004-T-G

42632576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47286990-A-T

42632645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: stop gained
orthologous variants: 47286921-C-T

42632699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47286867-C-T

42632786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47286779-T-C

42633223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47286626-G-A

42633223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47286626-G-T

42634084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47286169-T-C

42634104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47286149-T-A

42635316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47285127-T-G

42635350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47285093-T-A

42635350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47285093-T-C

42635374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47285011-A-G

http://identifiers.org/hco/6/GRCh38#42635622-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47284778-A-C

42635639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284761-A-T

http://identifiers.org/hco/6/GRCh38#42635651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47284750-C-A

42635651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284750-C-G

42635651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284750-C-T

42635803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284708-A-T

42636091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284460-A-G

http://identifiers.org/hco/6/GRCh38#42636162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47284406-C-A

42636582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284359-A-G

42636615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284329-T-C

42636861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47284086-T-C

42637447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47283498-G-C

42637468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47283484-T-C

42637498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47283455-T-G

42637662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47283328-A-G

42637713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47283290-G-T

42639322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47282034-G-A

http://identifiers.org/hco/6/GRCh38#42639346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47282010-A-C

42639464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281892-G-A

42639515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281820-T-G

42639525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281810-G-A

42639750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281545-T-C

42639887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281440-G-C

42639929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281392-G-A

42639944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281366-C-T

42640054-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281267-T-G

42640100-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281198-T-A

42640105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281193-A-G

42640127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281162-A-G

http://identifiers.org/hco/6/GRCh38#42640138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47281151-A-C

42640143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281146-T-C

42640148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281141-T-C

42640171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281122-T-C

42640171-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47281122-T-G

42640203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47281092-A-T

42640367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47280928-G-A

42640367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47280928-G-T

42640412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47280896-G-A

42640487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47280843-C-T

http://identifiers.org/hco/6/GRCh38#42641729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47280072-C-A

42641729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47280072-C-T

42642175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279616-C-G

42642233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279568-C-T

http://identifiers.org/hco/6/GRCh38#42642304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47279510-C-A

42642307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279507-A-G

42642307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279507-A-T

42642318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279484-G-A

http://identifiers.org/hco/6/GRCh38#42642333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47279465-C-A

42642333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279465-C-T

42642357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279430-T-G

42642364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279425-G-T

http://identifiers.org/hco/6/GRCh38#42642365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47279424-A-C

42642393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279396-A-G

42642511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279279-G-A

42642535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279255-T-C

42642600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47279197-T-C

42643575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47278838-G-A

http://identifiers.org/hco/6/GRCh38#42643737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47278656-A-C

42643902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47278523-G-A

42643980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47278446-G-A

42644232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47278218-G-T

42644262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47278188-A-G

http://identifiers.org/hco/6/GRCh38#42644344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47278106-C-A

42644344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47278106-C-G

42644344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47278106-C-T

http://identifiers.org/hco/6/GRCh38#42644380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47278090-C-A

42644400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47278077-T-C

42644467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47278025-T-C

42644544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47277948-T-A

42644544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47277948-T-C

42644640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277898-T-C

42644640-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277898-T-G

42644643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277895-G-A

42644643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277895-G-T

42644649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277887-G-C

42644649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277887-G-T

42644659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277877-A-G

42644668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277868-T-C

42644798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277778-G-T

42645033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277523-C-T

42645199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277407-C-T

42645201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277405-T-A

http://identifiers.org/hco/6/GRCh38#42645385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47277265-C-A

http://identifiers.org/hco/6/GRCh38#42645408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47277243-C-A

42645426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47277226-A-G

42645535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47277120-A-G

http://identifiers.org/hco/6/GRCh38#42645635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47277028-C-A

http://identifiers.org/hco/6/GRCh38#42645756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47276953-A-C

42645757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47276952-A-G

http://identifiers.org/hco/6/GRCh38#42648036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47275812-A-C

42648036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47275812-A-G

42648259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47275439-A-G

42648319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47275382-T-A

42650068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274917-C-T

http://identifiers.org/hco/6/GRCh38#42650203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47274776-C-A

42650203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274776-C-G

42650291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47274707-G-A

42650411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274588-G-A

42650411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274588-G-T

42652077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274065-T-A

http://identifiers.org/hco/6/GRCh38#42652139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47274007-C-A

42652139-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47274007-C-G

http://identifiers.org/hco/6/GRCh38#42652153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47273993-C-A

42652191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47273978-G-T

42655572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47270541-T-C

42655672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47270439-A-G

42655687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47270424-C-T

42656850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268717-C-G

42656850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268717-C-T

42656870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268696-G-A

42657918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268435-A-T

42657926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268427-T-C

42658000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47268360-G-A

42658566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47267743-T-G

42658828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47267478-A-G

42658828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47267478-A-T

http://identifiers.org/hco/6/GRCh38#42658832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47267474-A-C

42658832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 47267474-A-G

42659845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: synonymous variant
orthologous variants: 47266716-T-C

42662007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47266053-T-C

42662283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265788-G-A

42662283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265788-G-T

42662322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265751-G-A

42662322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265751-G-C

42662322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265751-G-T

42662358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265711-G-A

42662358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265711-G-T

42662359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265710-A-G

42662368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265697-A-G

42662371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265694-G-A

42662371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265694-G-C

42662371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265694-G-T

42662562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265490-G-A

42662562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265490-G-C

42662573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265466-A-G

42662610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265433-A-G

42662702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265352-C-G

42662808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265286-C-T

42663090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265142-C-G

42663205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265035-T-C

42663205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265035-T-G

42663215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265025-A-T

42663217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265023-A-G

http://identifiers.org/hco/6/GRCh38#42663222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47265018-C-A

42663222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47265018-C-T

http://identifiers.org/hco/6/GRCh38#42663564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47264682-A-C

42663698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47264530-T-G

42663929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47264455-T-G

42664013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47264389-C-G

42664013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47264389-C-T

42664571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47263974-T-C

42664809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47263773-A-G

42664828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47263754-C-T

42664908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47263681-C-T

42665235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47263435-A-G

http://identifiers.org/hco/6/GRCh38#42665348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47262969-A-C

42665354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47262963-T-C

42665372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47262946-T-A

http://identifiers.org/hco/6/GRCh38#42665380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47262938-C-A

42665380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47262938-C-T

42665461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, missense_variant
orthologous variants: 47262857-T-G

42665928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259847-T-C

42665974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259797-T-C

42665974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259797-T-G

42666021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259752-A-G

42666170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense_variant, stop_lost
orthologous variants: 47259572-A-T

42666277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259465-G-A

42666277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259465-G-T

42666315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259430-G-A

42666315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259430-G-T

42666387-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47259346-G-T

42670038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47257139-T-G

42670041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47257136-G-T

42670251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47256931-T-C

42670619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47256066-A-G

http://identifiers.org/hco/6/GRCh38#42670698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47255987-C-A

http://identifiers.org/hco/6/GRCh38#42673725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47255872-C-A

42673725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47255872-C-G

42673842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47255760-G-A

42673842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47255760-G-C

http://identifiers.org/hco/6/GRCh38#42673991-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47255608-C-A

42673991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47255608-C-T

42674238-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron_variant, undefined
orthologous variants: 47255387-A-T

42676122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47254330-G-A

42676122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: stop gained
orthologous variants: 47254330-G-T

42676141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47254311-A-G

42676141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47254311-A-T

42676164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47254288-A-G

42676328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47254217-G-T

http://identifiers.org/hco/6/GRCh38#42676330-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47254215-A-C

42676330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47254215-A-G

42676442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47254119-A-G

42676458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47254103-G-A

42676459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47254102-A-G

42676667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47253851-G-T

42676739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47253776-C-T

42676995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47253503-G-T

42677319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47253081-C-T

42677931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47252556-G-A

http://identifiers.org/hco/6/GRCh38#42678388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47252208-C-A

42678485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47252109-G-A

http://identifiers.org/hco/6/GRCh38#42678500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47252094-C-A

42678522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47252075-T-C

42678694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47251904-G-A

42679678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47250375-T-C

http://identifiers.org/hco/6/GRCh38#42679895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47250165-C-A

http://identifiers.org/hco/6/GRCh38#42683037-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47249648-C-A

42683037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47249648-C-T

http://identifiers.org/hco/6/GRCh38#42683125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47249560-C-A

42683212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47249479-G-A

42684744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47246482-A-G

http://identifiers.org/hco/6/GRCh38#42684745-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47246481-A-C

42684763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47246462-G-A

42684763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47246462-G-C

42684984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47246257-G-C

42684984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47246257-G-T

42688358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: missense variant
orthologous variants: 47245027-T-C

42689540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 47243506-T-C

42689679-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243368-C-G

42689679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243368-C-T

42689705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243342-C-T

42689720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243328-G-A

http://identifiers.org/hco/6/GRCh38#42689735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47243313-C-A

42689735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243313-C-T

42689752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243286-A-T

42689780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243244-A-G

42689818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47243206-G-T

42690961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47241489-C-T

42690986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47241464-G-A

42690986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: intron variant
orthologous variants: 47241464-G-T

http://identifiers.org/hco/6/GRCh38#42691329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47241113-C-A

http://identifiers.org/hco/6/GRCh38#42691370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47241085-C-A

http://identifiers.org/hco/6/GRCh38#42691588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47240902-C-A

42691588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47240902-C-T

42691653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47240842-T-C

42691653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47240842-T-G

42691703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47240795-G-T

http://identifiers.org/hco/6/GRCh38#42692276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47240379-C-A

http://identifiers.org/hco/6/GRCh38#42692284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47240371-C-A

http://identifiers.org/hco/6/GRCh38#42692291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47240364-C-A

42692291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47240364-C-T

42692352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47240306-G-A

42692352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47240306-G-T

42692393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47240276-G-A

http://identifiers.org/hco/6/GRCh38#42692631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47240062-C-A

42692698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47240022-C-T

http://identifiers.org/hco/6/GRCh38#42692834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239900-C-A

42692834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 47239900-C-T

http://identifiers.org/hco/6/GRCh38#42692914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239832-C-A

42692914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47239832-C-T

http://identifiers.org/hco/6/GRCh38#42693064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239694-A-C

http://identifiers.org/hco/6/GRCh38#42693080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239624-C-A

42693080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47239624-C-G

42693080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: 47239624-C-T

http://identifiers.org/hco/6/GRCh38#42693230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239459-C-A

http://identifiers.org/hco/6/GRCh38#42693387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21289
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#47239328-A-C