49444956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59677944-A-G

49445000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59677897-G-A

49445264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59677678-C-G

49445430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59677537-A-G

49450404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59676449-T-C

49450527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59676266-C-T

49450600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59676208-T-G

49450635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59676186-G-A

49450881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59675770-T-G

49451049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59675656-A-G

http://identifiers.org/hco/13/GRCh38#49451667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59675098-C-A

http://identifiers.org/hco/13/GRCh38#49451818-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59674954-C-A

49451818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59674954-C-T

http://identifiers.org/hco/13/GRCh38#49451853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59674936-C-A

49451853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 59674936-C-T

http://identifiers.org/hco/13/GRCh38#49451923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59674870-C-A

49451923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59674870-C-G

49451923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59674870-C-T

49455527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59673182-T-G

49456630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59671039-G-C

49456671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59671000-G-A

49456743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59670904-A-G

49456946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59670843-T-C

http://identifiers.org/hco/13/GRCh38#49457022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59670768-C-A

49457022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59670768-C-T

49457193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59670510-G-T

49459848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59669186-G-A

49459932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668869-T-C

http://identifiers.org/hco/13/GRCh38#49459941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59668860-C-A

49459994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668804-A-G

http://identifiers.org/hco/13/GRCh38#49460046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59668751-C-A

49460046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668751-C-G

49460285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668541-A-G

49460289-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668537-T-A

49460289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59668537-T-C

49460436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665511-C-T

49460541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665361-C-T

49460542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665360-A-G

http://identifiers.org/hco/13/GRCh38#49460548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59665354-C-A

49460548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665354-C-T

49460655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665281-A-G

49460655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59665281-A-T

http://identifiers.org/hco/13/GRCh38#49461101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/14/GRCm39#59663997-C-A

49461241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663870-G-A

49461241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663870-G-T

49461279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663832-A-G

49461279-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663832-A-T

49461297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663814-A-T

http://identifiers.org/hco/13/GRCh38#49461425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59663744-A-C

49461425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663744-A-T

49461524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663643-G-T

49461718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59663471-A-G

http://identifiers.org/hco/13/GRCh38#49461857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59663210-A-C

49462684-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662442-G-C

49462686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59662440-T-C

49467441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59661345-A-G

http://identifiers.org/hco/13/GRCh38#49467558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59661222-A-C

49467583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59661197-A-G

http://identifiers.org/hco/13/GRCh38#49467788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59661008-A-C

49467853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660942-T-G

49467874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59660921-T-C

49467874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59660921-T-G

http://identifiers.org/hco/13/GRCh38#49467954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59660841-C-A

49467954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59660841-C-T

49467985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660819-T-A

49467985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660819-T-G

49468323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660652-T-G

49468455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660543-G-A

49468617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660489-T-C

49468638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660471-T-G

49469012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59660039-T-G

http://identifiers.org/hco/13/GRCh38#49476320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59657168-A-C

http://identifiers.org/hco/13/GRCh38#49476335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59657153-C-A

http://identifiers.org/hco/13/GRCh38#49476509-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59656975-A-C

http://identifiers.org/hco/13/GRCh38#49476624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59656860-C-A

49476624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59656860-C-G

49476624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59656860-C-T

http://identifiers.org/hco/13/GRCh38#49477058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59656429-C-A

49477058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656429-C-T

49477087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656401-A-T

http://identifiers.org/hco/13/GRCh38#49477088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59656400-C-A

49477088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656400-C-T

49477093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656395-G-A

49477093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59656395-G-T

49480259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59654932-A-G

49480501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59654418-G-A

49480777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653471-C-G

49480857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653415-G-T

49480859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653413-T-A

49480859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653413-T-C

49480859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653413-T-G

http://identifiers.org/hco/13/GRCh38#49480999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59653263-C-A

49480999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 59653263-C-T

49481019-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59653243-T-A

49481065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59653197-G-A

49481134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653125-T-C

49481141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59653118-T-G

49482196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 59652094-G-T

49482208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59652082-C-T

49482233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59652057-T-C

49482288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59651497-G-A

49482301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59651489-T-G

http://identifiers.org/hco/13/GRCh38#49482356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59651435-A-C

49482397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59651415-A-G

49482659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59651193-G-A

49482659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59651193-G-T

49482792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 59651074-G-A

49482862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59651001-G-A

http://identifiers.org/hco/13/GRCh38#49482955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59650935-C-A

49482955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59650935-C-G

49482977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59650913-A-G

http://identifiers.org/hco/13/GRCh38#49482982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59650908-C-A

49483098-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59650822-T-G

49485709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59649552-C-G

49485709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59649552-C-T

http://identifiers.org/hco/13/GRCh38#49485720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59649541-C-A

49485887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649409-G-A

49485887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649409-G-T

49485903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649393-T-C

49485903-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649393-T-G

49485974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649323-T-C

49486441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649165-A-G

49486518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649100-G-T

49486553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649068-G-A

49486553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649068-G-T

49486561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649060-C-T

49486587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59649034-C-T

49486722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648848-C-G

49486886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648700-A-G

49487068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648523-A-G

49487171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648447-A-G

49487186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648432-C-G

49487264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648342-G-A

49487264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59648342-G-T

49487541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59647997-C-G

49487806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59647431-A-T

49487945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59647301-G-C

http://identifiers.org/hco/13/GRCh38#49487957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59647289-A-C

49488025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59647221-A-T

49488238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59647020-C-T

http://identifiers.org/hco/13/GRCh38#49488249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59647008-C-A

49488292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59646963-G-C

49488292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59646963-G-T

49488309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59646946-T-C

49488327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59646928-T-C

49488331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59646924-C-T

49488380-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59646875-C-G

http://identifiers.org/hco/13/GRCh38#49488384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59646871-A-C

49488419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59646836-A-G

49488754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59646563-A-G

49488821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59646517-T-A

49488833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59646513-G-T

http://identifiers.org/hco/13/GRCh38#49488894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59646453-C-A

49488894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59646453-C-G

49488894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59646453-C-T

49490464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644495-C-G

49490496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644462-T-C

49490500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644458-C-T

49490557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644402-G-T

49490737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644234-A-G

49490831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59644172-T-G

49490882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 59644121-T-A

49490947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644051-G-A

49490947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59644051-G-T

49491304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59643950-T-C

49491604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639996-G-A

49491604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639996-G-T

49491631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639968-T-G

49491646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639956-A-T

49491671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639928-T-A

49491671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639928-T-C

49491702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639892-T-A

http://identifiers.org/hco/13/GRCh38#49491714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59639880-C-A

49491714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59639880-C-G

http://identifiers.org/hco/13/GRCh38#49491724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59639871-C-A

49491724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59639871-C-T

49491745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59639850-A-G

49491780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 59639815-T-C

49491782-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59639813-G-C

49491906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59639705-G-A

49491906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59639705-G-T

49491952-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59639654-T-A

http://identifiers.org/hco/13/GRCh38#49494710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59635525-C-A

49494717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635518-A-G

49494747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635489-A-G

49494763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635473-G-A

49494788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635455-G-T

49494794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635449-C-T

49494823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635424-A-T

49494850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635395-A-G

49494857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635388-C-T

http://identifiers.org/hco/13/GRCh38#49494887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#59635368-C-A

49494891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635364-T-G

49494907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635345-A-T

49494910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59635342-A-G

49494916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59635336-A-G

49494925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635327-A-G

49494966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635286-T-C

49494969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20263
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59635283-G-A