43286805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 121946565-G-T

43287440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121947099-A-G

43287440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121947099-A-T

43287717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121947386-G-A

43287717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121947386-G-T

43287775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121947441-C-T

http://identifiers.org/hco/3/GRCh38#43288276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121948053-A-C

43288355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121948223-A-G

43288645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121948520-A-G

43289128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, undefined
orthologous variants: 121949252-A-G

43289129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, undefined
orthologous variants: 121949253-C-T

43289316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949363-G-A

43289534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949533-G-C

43289543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949542-C-T

http://identifiers.org/hco/3/GRCh38#43289637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121949649-C-A

43289769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121949778-C-G

http://identifiers.org/hco/3/GRCh38#43289785-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121949794-C-A

43289805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949813-G-A

43289805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949813-G-T

43289814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949821-G-A

43289814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949821-G-T

43289856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949860-T-C

43289933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949923-T-C

43289965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121949953-C-G

43290040-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950026-C-G

43290043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950029-G-A

43290091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950076-G-T

43290098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950083-T-C

43290562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950489-G-C

43290574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950501-G-C

http://identifiers.org/hco/3/GRCh38#43290606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121950535-A-C

43291012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121950898-G-A

43291277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121951188-T-G

43291841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121951404-G-A

43292521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121953268-A-G

43293287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121953647-C-T

43293492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121953772-A-G

43293541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121953820-A-G

43294296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121954408-A-G

43294945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121954967-T-C

43295125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121955116-A-G

43295332-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121955308-C-G

43295445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121956886-C-G

43295514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121956953-A-G

43296465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121957591-T-G

43296532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121957646-A-G

43296944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121958023-C-G

43297076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121958166-C-G

43297294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 121958321-A-G

43298173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121959751-G-A

43298427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121959998-A-T

43298540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960081-G-A

43298540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960081-G-T

43298661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960184-G-A

43298778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960296-T-C

43298878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960374-G-C

43299037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960506-T-C

43299222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960675-G-C

43299678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121960884-G-T

43299829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121961022-A-G

http://identifiers.org/hco/3/GRCh38#43299843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121961036-C-A

43299843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121961036-C-T

43300601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121961865-G-T

43300670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121961904-G-A

43300868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121962102-T-A

43300942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121962349-C-T

43300998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121962542-C-G

43301138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121962700-A-G

43301338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121962890-G-T

43302037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121963561-T-A

43302037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121963561-T-C

43302784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121965698-A-G

43303220-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 121966095-G-C

http://identifiers.org/hco/3/GRCh38#43303837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121966709-C-A

43303876-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121966741-T-G

43304395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967226-T-C

43304435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967264-C-T

43304561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967385-G-A

43304725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967543-T-A

43304865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967675-T-C

43304884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967694-A-G

43304913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967720-C-T

43304943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967750-T-G

43305240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121967973-C-T

43305312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121968076-G-A

43305357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121968106-C-T

43306000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

43306125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

43306229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/3/GRCh38#43310598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121968974-A-C

43310746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969085-G-A

43311004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969336-G-T

43311026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969357-A-G

43311026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969357-A-T

43311083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969414-A-G

43311394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969640-C-G

http://identifiers.org/hco/3/GRCh38#43311569-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121969818-A-C

43311603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969851-G-C

43311745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121969952-C-T

43312056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970183-G-A

43312306-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970486-C-G

43312513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970679-A-G

43312597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970739-A-G

43312598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970740-T-C

43312603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121970745-C-T

43313113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121971240-C-T

43313458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121971618-T-A

43313458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121971618-T-C

43313611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121971757-C-T

43317965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121972328-G-C

43317989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121972351-G-A

43318249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121972585-C-G

43318249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121972585-C-T

43320369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974419-A-G

43320369-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974419-A-T

43320372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974422-C-T

43320481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974509-C-T

43320581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974604-C-T

43320655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974679-G-A

43320806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974806-G-A

43320806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974806-G-T

43320951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974895-G-T

43320954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974898-A-G

43320954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974898-A-T

43321088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121974976-C-T

43321607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121975606-G-A

43322244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121975983-A-G

43326282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121978666-G-A

43326480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121978827-G-C

43326493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121978840-C-T

43326627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121978965-T-A

43326712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979044-G-A

43326765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979109-A-G

43326782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979126-T-C

43327277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979702-G-A

43327278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979703-A-G

43327346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979747-A-G

43327347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979748-T-C

43327616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121979980-A-G

43327792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980126-A-G

43327957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980294-G-T

43327990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980334-A-T

43328017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980361-A-T

43328086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980428-T-C

43328183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121980520-T-C

43330533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121984734-A-G

43330576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121984756-G-T

43330892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121984979-C-T

43331050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121985090-A-G

43331227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121985285-T-C

43331697-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121985860-C-G

43331697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121985860-C-T

43332118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121986170-T-G

43332290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121986343-T-C

43332334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986380-A-G

43332342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986389-G-A

43332495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986509-G-A

43332495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986509-G-C

43332495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986509-G-T

43332627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986613-T-G

http://identifiers.org/hco/3/GRCh38#43332728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121986707-C-A

43332728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986707-C-G

http://identifiers.org/hco/3/GRCh38#43332780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121986780-C-A

43332815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986816-G-T

http://identifiers.org/hco/3/GRCh38#43332919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121986893-A-C

43332928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121986902-G-A

http://identifiers.org/hco/3/GRCh38#43333052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121987011-A-C

43340248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121989350-A-G

43340252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121989354-G-A

43340299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 121989401-G-A

43341571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990102-T-C

43341675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990186-G-C

43341675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990186-G-T

http://identifiers.org/hco/3/GRCh38#43341739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121990247-C-A

43341739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990247-C-T

http://identifiers.org/hco/3/GRCh38#43341869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121990380-A-C

43341913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990418-A-G

43341990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990463-C-T

43341991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990464-G-A

43342003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121990475-G-A

43343230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron variant
orthologous variants: 121992880-T-G

43343560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121993189-A-G

43343560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121993189-A-T

43343622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121993257-G-A

43343622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121993257-G-C

43343633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121993268-G-A

http://identifiers.org/hco/3/GRCh38#43347308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121995279-C-A

43347436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995399-C-T

43347570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995533-T-C

43347618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995581-G-C

43347831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995794-A-G

43347867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995830-C-T

43347882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995845-G-A

43347882-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995845-G-C

43347894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995857-T-C

43347897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995860-T-C

43347933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995896-C-T

43347948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995911-C-G

43347948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121995911-C-T

43347956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995919-G-A

43347956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995919-G-T

43348027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995987-A-G

43348033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995993-G-C

43348033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121995993-G-T

43348071-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996031-T-G

http://identifiers.org/hco/3/GRCh38#43348107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996064-C-A

http://identifiers.org/hco/3/GRCh38#43348115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996072-C-A

43348122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996079-T-A

43348122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996079-T-C

43348122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996079-T-G

http://identifiers.org/hco/3/GRCh38#43348140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996097-C-A

43348140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996097-C-T

43348167-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996139-C-G

43348167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996139-C-T

43348170-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996142-T-A

43348170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996142-T-C

43348175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996147-G-A

43348207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996179-A-G

43348225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996197-T-C

43348225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996197-T-G

43348308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 121996274-T-C

43348310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 121996276-C-T

http://identifiers.org/hco/3/GRCh38#43348329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996295-C-A

43348329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996295-C-T

http://identifiers.org/hco/3/GRCh38#43348386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996310-C-A

43348386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996310-C-G

43348411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996323-T-C

43348447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996359-G-A

43348482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 121996394-T-A

http://identifiers.org/hco/3/GRCh38#43348495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996407-C-A

43348495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996407-C-T

43348496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996408-G-A

43348502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996414-C-G

43348502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996414-C-T

43348544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996456-G-A

43348591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996473-G-T

43348611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996482-G-A

43348611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996482-G-C

http://identifiers.org/hco/3/GRCh38#43348747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996552-C-A

43348973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996769-G-A

43348973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996769-G-T

43348979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996775-T-A

43348979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996775-T-C

43348980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996776-G-A

http://identifiers.org/hco/3/GRCh38#43349001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996797-C-A

43349001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996797-C-T

43349002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996798-G-A

43349002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996798-G-T

43349018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996814-G-T

43349037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996833-C-T

http://identifiers.org/hco/3/GRCh38#43349049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996839-C-A

43349051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996841-G-A

43349051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996841-G-C

43349051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996841-G-T

http://identifiers.org/hco/3/GRCh38#43349123-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996888-A-C

43349133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996898-G-A

43349133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996898-G-T

http://identifiers.org/hco/3/GRCh38#43349184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121996947-C-A

43349184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996947-C-T

43349194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996957-T-C

43349227-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121996988-C-G

http://identifiers.org/hco/3/GRCh38#43349245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121997006-C-A

43349330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997085-G-T

http://identifiers.org/hco/3/GRCh38#43349377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121997160-C-A

43349451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997248-T-C

43349561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997362-A-G

http://identifiers.org/hco/3/GRCh38#43349847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121997565-C-A

43349847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997565-C-G

43349847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997565-C-T

43349900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997616-G-A

43349900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997616-G-T

43349908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997622-C-T

43349913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997627-G-A

43349913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997627-G-T

43349973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121997681-T-C

43350029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997717-C-T

43350180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997855-T-C

43350180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997855-T-G

http://identifiers.org/hco/3/GRCh38#43350182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121997857-C-A

43350217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997892-G-A

43350217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997892-G-T

43350234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997907-G-A

43350326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121997991-G-A

43350339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998004-G-A

43350339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998004-G-T

43350354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998017-G-T

43350399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998056-G-A

43350516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998170-G-A

43350547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998200-A-G

43350650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 121998306-G-T

43351342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 121998976-A-G

http://identifiers.org/hco/3/GRCh38#43351464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#121999077-C-A

43351464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 121999077-C-T

http://identifiers.org/hco/3/GRCh38#43363038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122002110-C-A

43363298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002371-G-A

43363434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002501-T-C

43363545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002599-G-T

http://identifiers.org/hco/3/GRCh38#43363703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122002740-A-C

43363703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002740-A-T

43363750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002767-A-T

43363756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122002769-G-A

43364224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003274-T-C

43364238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003288-G-A

43364273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003332-C-T

43364296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003355-C-T

http://identifiers.org/hco/3/GRCh38#43364396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122003459-C-A

43364531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003576-T-G

43364741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003785-G-A

43364867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122003889-C-T

43365163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004117-C-T

43365164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004118-G-A

43365164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004118-G-T

43365189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004135-T-G

43365561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004428-G-C

43365726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004509-C-T

43365736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122004519-G-A

43365983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004702-G-T

43366004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004722-G-C

43366031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004749-A-G

43366031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004749-A-T

43366036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004754-G-A

43366036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004754-G-T

43366155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 122004824-G-T

http://identifiers.org/hco/3/GRCh38#43366224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122004853-C-A

http://identifiers.org/hco/3/GRCh38#43366292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122004907-C-A

43366292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122004907-C-T

43366341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122004960-A-G

43366421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005024-G-C

http://identifiers.org/hco/3/GRCh38#43366448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005043-C-A

43366448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005043-C-T

http://identifiers.org/hco/3/GRCh38#43366461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005053-C-A

43366461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005053-C-G

43366461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005053-C-T

http://identifiers.org/hco/3/GRCh38#43366480-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005076-C-A

43366617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005208-G-T

43366665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005259-G-A

43366665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005259-G-T

43366672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005266-G-A

43366672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005266-G-C

43366672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005266-G-T

43366676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005270-G-A

43366676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005270-G-C

43366676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005270-G-T

43366785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005378-G-A

43366785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005378-G-T

43366859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005442-C-T

http://identifiers.org/hco/3/GRCh38#43366889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005464-C-A

43366889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 122005464-C-T

http://identifiers.org/hco/3/GRCh38#43366924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005494-C-A

43366924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 122005494-C-T

http://identifiers.org/hco/3/GRCh38#43366994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005564-C-A

43366994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005564-C-T

43367004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005574-G-T

http://identifiers.org/hco/3/GRCh38#43367017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005592-A-C

43367030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005609-G-A

43367030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005609-G-C

43367083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005660-T-A

43367091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122005668-A-G

http://identifiers.org/hco/3/GRCh38#43367116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122005690-C-A

43367717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006031-A-G

43367731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006045-C-T

43367774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006077-G-A

43368638-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006690-G-C

43368660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006712-T-C

43368817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006795-G-A

43368990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006937-G-A

43368999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122006946-G-A

43370547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122007493-T-G

43370570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122007513-G-A

43370940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122007784-G-A

43371014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122007824-C-T

43371164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122007954-C-G

43371272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122008048-A-G

http://identifiers.org/hco/3/GRCh38#43371277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122008053-C-A

43371308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122008084-G-A

43371461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122008229-C-T

43388450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122009475-C-T

43388874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011004-A-G

43389023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011154-C-T

43389200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011362-G-A

43389524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011660-G-A

43389546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011678-A-G

43389636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122011751-T-C

http://identifiers.org/hco/3/GRCh38#43389739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#122011840-C-A

43389854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 122011921-G-A

http://identifiers.org/hco/3/GRCh38#43390345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122012346-C-A

43390557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122012502-A-G

43390639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122012564-A-G

43390690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122012617-G-A

43391145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122013063-T-C

43391186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122013118-C-T

43405156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122019000-T-C

43405225-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122019049-T-A

43405285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122019110-G-C

43405801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122019987-T-C

43405850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122020033-T-C

http://identifiers.org/hco/3/GRCh38#43406191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122021098-C-A

43406402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122021300-A-G

43413826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122022412-C-T

43416043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122022549-T-G

http://identifiers.org/hco/3/GRCh38#43416212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122022708-A-C

http://identifiers.org/hco/3/GRCh38#43416463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#122022949-A-C

43416463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122022949-A-G

43416742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122023188-A-G

43418900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122024393-C-T

43419375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122024847-G-C

43419391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122024860-T-C

43420039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122025379-A-T

43423016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30598
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 122026215-T-C