http://identifiers.org/hco/15/GRCh38#30815342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55834608-C-A

30815381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55834647-G-A

30815478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55834736-G-A

30815478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55834736-G-T

30815639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55834884-C-T

30816222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835293-T-G

30816401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835461-G-A

30816401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835461-G-T

30816463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835522-T-C

30816464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835523-G-T

30816686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835738-G-A

30816686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835738-G-T

http://identifiers.org/hco/15/GRCh38#30816691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55835743-C-A

30816691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835743-C-T

30816705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835756-G-A

30816705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835756-G-T

30816742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835784-G-A

30816742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55835784-G-T

30817606-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838061-T-A

30817624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838085-T-G

30817936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838369-A-G

30817936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838369-A-T

30817980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838413-G-A

30817980-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838413-G-C

30817980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838413-G-T

http://identifiers.org/hco/15/GRCh38#30818034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55838467-C-A

30818034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55838467-C-G

30818120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838554-T-C

30818120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838554-T-G

30818124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838558-C-G

30818124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838558-C-T

30818126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838560-G-C

30818126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838560-G-T

30818192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838611-G-T

30818197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838616-G-A

30818197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838616-G-C

30818197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55838616-G-T

30822485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839491-T-C

30822561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55839566-G-A

30822561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55839566-G-T

30822724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839729-T-A

30822724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839729-T-C

30822729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839734-G-A

30822729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839734-G-C

30822729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839734-G-T

30822776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839780-G-A

30822776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839780-G-T

30822792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839793-A-G

30822822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839821-G-T

30822827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839825-T-A

30822841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839839-T-C

http://identifiers.org/hco/15/GRCh38#30822850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55839848-C-A

30822850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55839848-C-T

30823070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840183-G-A

30823113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840304-A-G

30823168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840360-A-G

30823424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840741-C-G

30823424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840741-C-T

30823542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840860-G-A

30823542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55840860-G-T

30823624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840942-G-A

30823624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840942-G-T

http://identifiers.org/hco/15/GRCh38#30823627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55840945-C-A

30823627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840945-C-T

30823637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840955-G-A

30823637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840955-G-C

30823637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55840955-G-T

http://identifiers.org/hco/15/GRCh38#30823672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841002-C-A

30823672-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841002-C-G

30823672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841002-C-T

30823700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841030-G-T

30823713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841043-T-A

30823713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841043-T-C

30823713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841043-T-G

http://identifiers.org/hco/15/GRCh38#30823729-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841059-C-A

30823729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841059-C-G

30823729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55841059-C-T

30823876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841198-T-A

30823876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841198-T-C

http://identifiers.org/hco/15/GRCh38#30823877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841199-C-A

30823877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841199-C-T

http://identifiers.org/hco/15/GRCh38#30823908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841229-A-C

http://identifiers.org/hco/15/GRCh38#30823915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841237-C-A

30823915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841237-C-G

30823915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841237-C-T

http://identifiers.org/hco/15/GRCh38#30823945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841267-C-A

30824306-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841299-T-A

30824306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841299-T-G

30824478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841424-G-A

http://identifiers.org/hco/15/GRCh38#30824628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841514-C-A

30824628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841514-C-G

30824628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55841514-C-T

http://identifiers.org/hco/15/GRCh38#30824763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55841649-C-A

30826177-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845499-A-T

30826348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845641-A-T

30826654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55845968-C-G

http://identifiers.org/hco/15/GRCh38#30827150-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55846423-A-C

30827184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846459-G-T

30827305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846549-A-G

30827548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846671-C-T

http://identifiers.org/hco/15/GRCh38#30827712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55846816-C-A

30827712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55846816-C-T

http://identifiers.org/hco/15/GRCh38#30827772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55846875-C-A

30827772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 55846875-C-T

30827878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846980-G-A

30827878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846980-G-T

http://identifiers.org/hco/15/GRCh38#30827897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55846999-C-A

30827897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846999-C-G

30827897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55846999-C-T

30832537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851616-C-T

30832557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851636-T-G

30832627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851707-C-T

30832690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851751-A-G

30832690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851751-A-T

30832692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851753-A-G

30832731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55851792-T-C

http://identifiers.org/hco/15/GRCh38#30832846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55851904-C-A

30832846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55851904-C-T

30832993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852007-G-T

30833280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852290-C-T

30833354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852392-G-A

http://identifiers.org/hco/15/GRCh38#30833356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55852394-C-A

30833361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852399-C-T

30833367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852405-G-A

30833717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55852917-G-A

30833913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853111-C-T

30833915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853113-C-T

30834065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853250-G-A

30834065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853250-G-C

30834231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853394-G-A

30834231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853394-G-T

30834284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853450-G-A

30834284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853450-G-T

30834309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853473-T-C

30834415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55853579-A-G

30834415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55853579-A-T

http://identifiers.org/hco/15/GRCh38#30834545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55853677-C-A

30834545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853677-C-T

30834721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853833-T-C

30834747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853861-G-A

30834798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853924-G-A

30834798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853924-G-C

30834798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853924-G-T

30834802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55853928-G-T

http://identifiers.org/hco/15/GRCh38#30834813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55853977-C-A

30834822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854006-G-A

30834822-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854006-G-C

30834822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854006-G-T

http://identifiers.org/hco/15/GRCh38#30834944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55854150-C-A

30834944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55854150-C-G

30834944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55854150-C-T

http://identifiers.org/hco/15/GRCh38#30834953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55854159-C-A

30834953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55854159-C-T

http://identifiers.org/hco/15/GRCh38#30835025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55854231-C-A

30835064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55854270-T-C

30835108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854317-A-G

http://identifiers.org/hco/15/GRCh38#30835120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55854329-C-A

30835120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854329-C-G

30835120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854329-C-T

http://identifiers.org/hco/15/GRCh38#30835142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55854352-C-A

30836038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854902-T-G

30836073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55854948-T-G

http://identifiers.org/hco/15/GRCh38#30836152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855018-C-A

30836152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855018-C-T

30836191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55855057-T-C

30836211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55855077-T-C

30836350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855216-A-G

30836350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855216-A-T

http://identifiers.org/hco/15/GRCh38#30836352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855218-A-C

30836352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855218-A-G

30836352-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855218-A-T

30836353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855219-G-A

30836353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855219-G-C

30836353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855219-G-T

30836370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855236-G-A

30836370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855236-G-T

30836385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855251-G-A

30836385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855251-G-T

30836392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855258-G-A

30836392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855258-G-T

http://identifiers.org/hco/15/GRCh38#30836416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855279-C-A

30836416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855279-C-T

30836434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855299-G-T

http://identifiers.org/hco/15/GRCh38#30836499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855365-A-C

30836518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855383-G-C

30836731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855591-G-A

30836731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855591-G-C

30836752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55855613-C-T

http://identifiers.org/hco/15/GRCh38#30836934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855817-A-C

30836934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55855817-A-T

http://identifiers.org/hco/15/GRCh38#30837002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55855861-A-C

30837435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856030-G-A

30837435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856030-G-T

http://identifiers.org/hco/15/GRCh38#30837441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55856037-C-A

30837441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856037-C-T

30837451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856047-A-G

30837573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 55856267-T-C

30837669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55856362-A-G

30837718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856410-A-T

30837733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856419-G-A

30837733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856419-G-C

30837733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55856419-G-T

http://identifiers.org/hco/15/GRCh38#30837931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55856614-C-A

30837931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55856614-C-G

30837931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55856614-C-T

30843887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857404-T-C

30843925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 55857424-T-C

30843978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55857472-A-G

30843978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55857472-A-T

http://identifiers.org/hco/15/GRCh38#30844015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#55857509-A-C

30844015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55857509-A-G

30844015-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55857509-A-T

30844120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39056
most severe consequence: non coding transcript exon variant
orthologous variants: 55857616-T-C