http://identifiers.org/hco/6/GRCh38#30914216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978529-C-A

30914216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 35978529-C-T

http://identifiers.org/hco/6/GRCh38#30914240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978506-C-A

http://identifiers.org/hco/6/GRCh38#30914249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978496-C-A

30914249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5 prime UTR variant
orthologous variants: 35978496-C-G

30914249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5 prime UTR variant
orthologous variants: 35978496-C-T

http://identifiers.org/hco/6/GRCh38#30914257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978488-C-A

30914257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 35978488-C-G

30914257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 35978488-C-T

30914264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 35978485-G-T

http://identifiers.org/hco/6/GRCh38#30914306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978473-C-A

30914306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35978473-C-T

http://identifiers.org/hco/6/GRCh38#30914354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978460-C-A

30914354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978460-C-T

30914355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978459-G-A

30914355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978459-G-T

30914361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978453-G-A

30914381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978439-G-A

30914443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978421-T-A

30914443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 35978421-T-C

30914554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978388-T-C

http://identifiers.org/hco/6/GRCh38#30914559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978383-C-A

30914559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978383-C-T

30914649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978299-G-A

30914649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978299-G-T

http://identifiers.org/hco/6/GRCh38#30914655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35978293-A-C

30914655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978293-A-G

30914655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978293-A-T

30914790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35978203-T-C

30914948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 35978052-C-T

30915004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35977996-G-A

30915004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35977996-G-C

30915004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35977996-G-T

30915073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35977934-G-C

30915123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35977876-T-G

http://identifiers.org/hco/6/GRCh38#30915159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35977812-C-A

30915159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35977812-C-T

30915211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35977760-T-C

30915211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35977760-T-G

30915218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35977753-G-A

30915244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35977724-A-G

30915390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35977610-C-G

30915390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35977610-C-T

30915476-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35977526-G-T

http://identifiers.org/hco/6/GRCh38#30915566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35977419-C-A

30915566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35977419-C-T

http://identifiers.org/hco/6/GRCh38#30915600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35977332-C-A

30915600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977332-C-T

30915615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977289-C-T

30915616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977288-C-T

http://identifiers.org/hco/6/GRCh38#30915618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35977286-C-A

30915618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977286-C-G

30915627-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977277-T-G

http://identifiers.org/hco/6/GRCh38#30915699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#35977199-C-A

30915699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35977199-C-T

30915874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35977014-G-T

30915964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35976946-G-A

30916000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35976910-C-G

30916151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 35976774-G-A

30916185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35976740-G-A

http://identifiers.org/hco/6/GRCh38#30916209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976716-C-A

30916209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35976716-C-T

http://identifiers.org/hco/6/GRCh38#30916311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976645-C-A

30916320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35976639-T-G

http://identifiers.org/hco/6/GRCh38#30916355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976604-C-A

30916405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35976508-A-G

30916425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35976488-G-A

30916425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35976488-G-T

30916429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976484-A-G

30916437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976476-T-A

30916438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976475-A-T

30916470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976416-G-A

30916470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976416-G-T

http://identifiers.org/hco/6/GRCh38#30916521-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976275-A-C

30916521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976275-A-G

30916521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976275-A-T

http://identifiers.org/hco/6/GRCh38#30916534-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976263-A-C

30916534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976263-A-G

30916534-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976263-A-T

30916547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976250-T-A

30916547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976250-T-C

30916547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976250-T-G

http://identifiers.org/hco/6/GRCh38#30916549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976248-C-A

30916549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976248-C-G

30916549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976248-C-T

http://identifiers.org/hco/6/GRCh38#30916551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35976246-A-C

30916551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976246-A-G

30916551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976246-A-T

30916553-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976244-T-A

30916555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976242-G-A

30916555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976242-G-C

30916555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35976242-G-T

30916654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975977-T-A

30916654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975977-T-C

30916654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975977-T-G

30916701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975900-T-C

30916707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975894-A-G

30916804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975810-T-C

30916805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35975809-G-A

30916906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35975714-C-T

30916912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35975708-C-G

30916978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975645-G-A

30916978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975645-G-C

30916978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975645-G-T

30917096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975514-T-A

30917096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975514-T-G

30917393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975284-C-T

30917556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975163-G-C

30917558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975161-G-A

30917558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975161-G-T

30917641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975122-G-C

30917641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975122-G-T

30917659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35975104-G-T

http://identifiers.org/hco/6/GRCh38#30917661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35975102-C-A

30917722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35975045-A-G

30917722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35975045-A-T

http://identifiers.org/hco/6/GRCh38#30917737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35975030-C-A

30917737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35975030-C-T

http://identifiers.org/hco/6/GRCh38#30917767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35975000-C-A

30917767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35975000-C-T

30917798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35974969-G-C

http://identifiers.org/hco/6/GRCh38#30917862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35974910-A-C

30917862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974910-A-G

http://identifiers.org/hco/6/GRCh38#30917879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35974895-C-A

30917879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974895-C-G

30917923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974877-T-C

30917923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974877-T-G

30917974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974838-T-C

30918004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron variant
orthologous variants: 35974809-G-A

30919678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35974056-T-C

30919678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35974056-T-G

30919704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35974036-G-C

30919704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35974036-G-T

http://identifiers.org/hco/6/GRCh38#30919715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35974026-C-A

30919715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35974026-C-T

http://identifiers.org/hco/6/GRCh38#30919751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35973991-C-A

30919778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35973964-T-C

30919795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973947-G-T

30919803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973939-C-T

30919818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973924-G-A

http://identifiers.org/hco/6/GRCh38#30919834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35973908-C-A

30919834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973908-C-T

30919859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35973883-G-T

30919898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35973865-G-A

30919898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35973865-G-T

http://identifiers.org/hco/6/GRCh38#30920075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35973133-C-A

30920091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35973118-G-A

30920091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35973118-G-T

http://identifiers.org/hco/6/GRCh38#30920112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35973097-C-A

30920112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973097-C-T

http://identifiers.org/hco/6/GRCh38#30920119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35973090-C-A

30920133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35973076-A-T

30920218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 35972990-T-G

30920313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972914-T-C

30920320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972907-G-A

30920320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972907-G-T

30920375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35972853-C-T

30920383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35972845-A-G

30920411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35972817-C-T

30920465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972765-G-A

30920465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972765-G-T

30920486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972745-A-G

http://identifiers.org/hco/6/GRCh38#30920538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972678-C-A

30920538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972678-C-T

30920566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972644-T-C

30920601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972601-G-A

30920601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972601-G-T

http://identifiers.org/hco/6/GRCh38#30920604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972598-C-A

http://identifiers.org/hco/6/GRCh38#30920716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972498-C-A

30920716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35972498-C-T

http://identifiers.org/hco/6/GRCh38#30920717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972497-C-A

30920717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35972497-C-T

http://identifiers.org/hco/6/GRCh38#30920737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972477-C-A

30920737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35972477-C-T

30920776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972439-G-A

http://identifiers.org/hco/6/GRCh38#30920780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972435-C-A

30920780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972435-C-T

30920781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972434-A-G

30920781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972434-A-T

30920832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972391-G-C

30920832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972391-G-T

30920836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972387-T-C

http://identifiers.org/hco/6/GRCh38#30920851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972336-C-A

30920851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972336-C-G

http://identifiers.org/hco/6/GRCh38#30920853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35972334-C-A

30920853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972334-C-T

30920944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35972182-G-T

30920996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971972-C-G

30920996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971972-C-T

30920999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971934-G-A

30920999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971934-G-T

http://identifiers.org/hco/6/GRCh38#30921006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971927-C-A

30921006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971927-C-G

30921016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971917-G-A

http://identifiers.org/hco/6/GRCh38#30921021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971912-C-A

30921021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971912-C-T

30921288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35971631-G-A

30921288-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35971631-G-C

30921366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971565-A-G

30921376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971561-A-G

30921450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971515-C-T

http://identifiers.org/hco/6/GRCh38#30921475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971495-A-C

30921475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971495-A-G

30921475-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971495-A-T

http://identifiers.org/hco/6/GRCh38#30921489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971481-C-A

30921489-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971481-C-G

30921489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971481-C-T

http://identifiers.org/hco/6/GRCh38#30921522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971449-A-C

30921522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971449-A-G

30921523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971448-C-T

http://identifiers.org/hco/6/GRCh38#30921540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971433-C-A

30921540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971433-C-G

30921540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971433-C-T

30921628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35971357-G-T

30921637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35971348-G-A

30921662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35971323-G-A

http://identifiers.org/hco/6/GRCh38#30921808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971253-C-A

http://identifiers.org/hco/6/GRCh38#30921864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35971234-A-C

30921966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35971133-C-T

30921996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 35971103-G-A

30921998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35971101-G-A

30922116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35971017-A-G

30922130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35971003-T-C

30922191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970942-C-T

30922217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35970916-C-T

30922255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970887-A-T

http://identifiers.org/hco/6/GRCh38#30922264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35970878-C-A

30922353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970857-T-A

30922353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970857-T-C

30922391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35970836-C-T

30922426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35970818-C-T

30922432-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35970812-A-T

30922437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35970807-T-C

http://identifiers.org/hco/6/GRCh38#30922440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35970804-C-A

30922543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970701-G-A

30922543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970701-G-T

30922605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35970644-G-T

30922752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970564-T-C

30922754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970562-G-A

http://identifiers.org/hco/6/GRCh38#30922789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35970528-C-A

30922789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970528-C-T

http://identifiers.org/hco/6/GRCh38#30922856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35970484-C-A

30922857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970483-C-T

http://identifiers.org/hco/6/GRCh38#30922860-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35970480-A-C

30922913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970428-C-G

30923043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970309-G-A

30923043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970309-G-T

30923046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970306-C-T

30923094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970289-T-C

30923267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970143-T-C

30923283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970131-C-T

30923322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35970099-A-G

30923371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35970051-A-G

30923587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969847-G-A

30923587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969847-G-T

30923621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969819-G-T

30923646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969813-G-A

30923646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969813-G-T

30923698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969761-T-A

30923698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969761-T-G

30923724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969738-G-A

30923724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969738-G-T

30923784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969687-A-G

30923791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969680-G-A

30923791-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969680-G-C

30923791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969680-G-T

http://identifiers.org/hco/6/GRCh38#30923820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969654-C-A

30923820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969654-C-T

30923860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969607-T-C

30923864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969603-G-C

30923940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969544-G-A

30923940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969544-G-C

30923940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969544-G-T

http://identifiers.org/hco/6/GRCh38#30923944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969540-C-A

30923944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969540-C-T

http://identifiers.org/hco/6/GRCh38#30923948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969536-A-C

30923948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969536-A-G

30923948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969536-A-T

http://identifiers.org/hco/6/GRCh38#30924012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969492-C-A

30924012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969492-C-T

30924037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969467-T-A

30924060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969443-T-C

30924086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969439-T-G

http://identifiers.org/hco/6/GRCh38#30924146-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969405-C-A

30924146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969405-C-G

30924146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969405-C-T

30924154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35969398-T-C

30924378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35969204-C-T

30924468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35969114-G-C

30924547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35969035-G-A

30924547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35969035-G-T

30924565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35969017-G-A

30924565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35969017-G-C

http://identifiers.org/hco/6/GRCh38#30924567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969015-C-A

30924567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35969015-C-T

http://identifiers.org/hco/6/GRCh38#30924575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35969002-C-A

30924575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35969002-C-T

30924617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968941-G-T

30924618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968940-A-G

http://identifiers.org/hco/6/GRCh38#30924619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35968939-A-C

30924619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968939-A-G

30924624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968934-T-A

30924624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968934-T-C

30924624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968934-T-G

http://identifiers.org/hco/6/GRCh38#30924643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35968893-C-A

30924643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968893-C-T

30924775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968774-A-T

30925066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968378-C-T

30925282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 35968200-G-A

30925313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35968169-C-T

http://identifiers.org/hco/6/GRCh38#30925443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35968075-A-C

http://identifiers.org/hco/6/GRCh38#30925449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35968069-C-A

30925449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968069-C-G

30925449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968069-C-T

30925518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968050-G-C

30925518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35968050-G-T

http://identifiers.org/hco/6/GRCh38#30925564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35967995-C-A

30925594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35967965-T-C

30925624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35967935-G-A

30925624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35967935-G-T

http://identifiers.org/hco/6/GRCh38#30925636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35967923-C-A

30925830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35967788-G-A

30925840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35967778-C-G

30925881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35967747-G-A

30925881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 35967747-G-T

30925955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35967673-C-T

30925963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35967665-C-T

30925967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35967661-A-G

http://identifiers.org/hco/6/GRCh38#30925968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35967660-C-A

30925983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 35967645-A-G

30926032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35967613-A-G

http://identifiers.org/hco/6/GRCh38#30926275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#35967402-C-A

30926275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35967402-C-T

30926285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35967394-G-A

30926285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35967394-G-T

30926314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21642
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35967365-A-G