128685660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32460329-T-C

128686191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32459786-T-C

128686267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32459732-A-G

128686293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32459704-A-G

128686368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32459634-A-G

http://identifiers.org/hco/11/GRCh38#128686755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32459323-C-A

128686755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32459323-C-T

128687017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32459190-G-A

128687017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32459190-G-T

128687311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458994-A-G

128687710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458698-A-G

128687710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458698-A-T

128687789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458622-C-T

128687867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458555-T-C

128687920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458506-G-T

128688002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458427-G-C

128688307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32458128-C-T

128688444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32457993-C-G

128688639-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32457816-T-G

128688670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32457783-G-A

128689102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32457480-G-A

128689208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32457419-C-T

128689777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32456911-A-G

128689777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32456911-A-T

128689857-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32456809-C-G

128689878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32456786-C-T

128690733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455974-T-C

128690763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455946-T-A

128690810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455898-C-G

128690810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455898-C-T

128690962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455747-G-T

128691308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455373-C-T

128691329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455350-C-G

128691575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455135-G-T

http://identifiers.org/hco/11/GRCh38#128691613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32455110-C-A

128691660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32455056-G-T

128691757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454959-T-A

128691814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454902-T-C

128691816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454900-T-A

http://identifiers.org/hco/11/GRCh38#128691829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32454887-C-A

128691836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32454880-A-G

http://identifiers.org/hco/11/GRCh38#128691856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32454861-C-A

128691856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454861-C-T

128691858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454859-A-G

128691858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454859-A-T

128691867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454852-G-A

128691867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454852-G-T

128691936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32454782-A-G

128691977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32454741-T-C

http://identifiers.org/hco/11/GRCh38#128692000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32454717-C-A

128692000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32454717-C-T

http://identifiers.org/hco/11/GRCh38#128692201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32454568-C-A

128692201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32454568-C-G

128692488-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32454298-G-C

128692603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32454182-G-T

128692850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453938-A-T

128693014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453768-G-A

128693014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453768-G-T

128693016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453766-T-C

128693121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453676-A-G

128693121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453676-A-T

http://identifiers.org/hco/11/GRCh38#128693140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32453657-C-A

128693140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453657-C-T

128693153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453645-G-A

128693153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453645-G-T

128693214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453598-G-T

128693314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453504-G-A

128693314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32453504-G-T

http://identifiers.org/hco/11/GRCh38#128693418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32453435-C-A

http://identifiers.org/hco/11/GRCh38#128693503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32453238-C-A

128693503-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32453238-C-G

128693503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32453238-C-T

128693750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452996-C-T

http://identifiers.org/hco/11/GRCh38#128693776-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32452970-A-C

128693776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452970-A-G

128693832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32452915-A-G

128693869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32452881-G-A

128694291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452470-A-G

128694291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452470-A-T

http://identifiers.org/hco/11/GRCh38#128694330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32452441-C-A

128694330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452441-C-G

128694330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452441-C-T

http://identifiers.org/hco/11/GRCh38#128694359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32452416-C-A

http://identifiers.org/hco/11/GRCh38#128694374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32452401-C-A

128694374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452401-C-G

128694374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452401-C-T

128694376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452399-C-G

128694406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452369-G-A

128694457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452324-C-G

128694633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32452157-C-T

http://identifiers.org/hco/11/GRCh38#128694679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32452102-C-A

128694691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32452090-G-A

128695136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32451665-C-T

128695775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32450954-G-A

128695775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32450954-G-T

128695776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32450953-T-C

128695783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32450946-G-T

128695901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32450840-G-T

128695939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32450794-G-T

128695956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32450777-A-G

128696033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450699-G-A

128696033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450699-G-T

http://identifiers.org/hco/11/GRCh38#128696093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32450640-A-C

128696165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450568-G-T

128696315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450400-T-G

128696415-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450300-T-G

128696424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450292-T-C

128696669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450092-G-A

128696673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32450088-C-T

128696775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32449983-T-C

128696775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32449983-T-G

128697271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32449537-G-T

http://identifiers.org/hco/11/GRCh38#128697837-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32449051-A-C

128697960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448966-A-G

128697985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448937-C-T

128698003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448917-A-G

128698146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448839-C-G

128698152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448833-G-C

128698209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448809-G-A

128698619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448527-G-A

128699121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448078-A-G

128699166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32448029-G-A

128699597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32446836-T-G

128700529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32446170-G-C

128701465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32445297-C-G

http://identifiers.org/hco/11/GRCh38#128701533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32445232-C-A

128701847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444941-C-T

128701848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444940-G-A

128702097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444696-T-A

128702140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444653-A-G

128702498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444160-G-A

128702693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32444009-C-T

128702976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32443922-A-G

128703217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32443706-G-C

128704107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32443040-A-G

128704499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32442678-A-G

128704742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32442413-C-T

128704810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32442347-G-A

128705077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32442055-T-C

128705087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32442045-T-A

128705154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32441909-A-G

128705433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32441405-T-C

128705524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32441315-A-G

128705659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32441183-G-A

128706570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440672-G-T

128706621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440621-C-G

128706639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440604-A-G

128706736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440516-T-A

128707054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440209-G-T

128707072-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440196-G-T

128707099-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440175-T-C

128707102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32440172-G-A

http://identifiers.org/hco/11/GRCh38#128707360-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32439935-A-C

http://identifiers.org/hco/11/GRCh38#128707630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32439690-A-C

128708268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32439072-G-A

128708314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32439026-T-A

128708700-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32438605-C-G

128708700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32438605-C-T

128709298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32437572-C-T

http://identifiers.org/hco/11/GRCh38#128709311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32437567-C-A

128709311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32437567-C-T

128709480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32437415-T-C

128709849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32436946-G-A

128709859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32436936-G-A

http://identifiers.org/hco/11/GRCh38#128710020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32436733-C-A

128710269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32436258-G-A

128710604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32435912-T-C

128710914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32435033-G-A

128710930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32435017-T-C

128710955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434992-C-G

128711492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434259-T-C

128711526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434222-C-T

128711554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434194-C-T

128711583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434165-A-G

128711596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434152-A-G

128711607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434140-C-T

128711629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434117-T-C

128711663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32434085-A-G

128712816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433759-T-C

128712854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433721-C-G

128713311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433271-T-C

128713454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433143-A-G

128713542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433056-A-G

128713590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32433008-T-A

http://identifiers.org/hco/11/GRCh38#128714115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32432479-C-A

128714401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32432228-T-C

128714565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32432058-G-A

128714565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32432058-G-C

128714644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431991-T-A

128714754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431925-G-A

128714754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431925-G-T

http://identifiers.org/hco/11/GRCh38#128715130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32431784-C-A

128715304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431611-T-C

128715313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431602-C-G

128715496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32431407-A-G

128716266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32430642-T-C

128716425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32430482-G-A

http://identifiers.org/hco/11/GRCh38#128716460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32430447-C-A

128716460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32430447-C-G

128716460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32430447-C-T

128716876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32430070-A-G

128717010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32429924-C-G

128717014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32429912-C-T

128717495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32429391-C-T

128717649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32429252-G-T

http://identifiers.org/hco/11/GRCh38#128717820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32429125-C-A

128717965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428959-T-G

128717981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428943-G-C

128717984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428934-T-C

128718050-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428895-T-A

128718050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428895-T-C

128718310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428700-G-A

128718398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32428657-G-A

http://identifiers.org/hco/11/GRCh38#128718532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32428526-A-C

128719049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32428020-A-G

http://identifiers.org/hco/11/GRCh38#128719257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32427808-C-A

http://identifiers.org/hco/11/GRCh38#128719293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32427775-C-A

http://identifiers.org/hco/11/GRCh38#128719400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32427661-A-C

128719400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32427661-A-G

128719422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32427635-T-C

128719603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32427487-C-T

128719624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32427466-G-T

128720011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32426787-T-G

128720361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32426343-A-G

128720423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32426291-G-A

128720423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32426291-G-C

128720488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32426227-C-T

128720489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32426226-A-G

128720493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32426225-A-G

128721335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32425415-G-A

128721335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32425415-G-T

128721457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32425270-C-T

128721536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32425215-C-T

128721591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32425172-A-G

http://identifiers.org/hco/11/GRCh38#128721883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32424802-A-C

128721890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424793-A-G

128722129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424609-G-A

128722276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424509-G-A

128722276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424509-G-C

128722628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424173-G-T

128722665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424061-A-G

128722666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424060-C-G

128722666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32424060-C-T

128722864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423679-G-A

128722901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423654-T-C

128722901-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423654-T-G

128722966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423589-G-T

128723017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423538-G-C

128723029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423505-G-C

http://identifiers.org/hco/11/GRCh38#128723129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32423415-C-A

128723129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423415-C-T

128723144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423390-A-G

128723144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423390-A-T

128723172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423361-G-C

http://identifiers.org/hco/11/GRCh38#128723189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32423346-C-A

http://identifiers.org/hco/11/GRCh38#128723266-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32423261-C-A

128723266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32423261-C-T

128724286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32422732-G-A

128724286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32422732-G-T

128724374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32422655-G-C

128724376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32422653-G-A

128724716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32422318-G-A

http://identifiers.org/hco/11/GRCh38#128724799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32422265-A-C

128725331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32421693-A-G

128725347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32421677-A-G

128725353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32421671-A-G

128725870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32421161-A-G

128725909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32421120-T-C

128726170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420867-A-G

128726242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420794-T-A

128726445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420607-A-G

128726495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420565-G-C

128726693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420422-C-T

128726696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32420419-G-A

128726918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32420186-G-A

128727388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419715-G-A

128727431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419674-G-A

128727457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419648-G-T

128727586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419521-C-T

128727756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419304-C-T

http://identifiers.org/hco/11/GRCh38#128727800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32419285-C-A

128727908-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32419175-T-G

128728083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418997-C-T

128728093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418987-A-G

128728260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32418796-T-C

128728312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418739-G-A

128728437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418631-T-A

128728603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418394-C-T

128728818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418191-A-G

128728836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418170-C-T

128728923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418044-G-A

128728923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32418044-G-T

128729077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32417897-T-A

http://identifiers.org/hco/11/GRCh38#128729193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32417819-A-C

128729209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32417803-A-T

128729854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32416824-A-T

128729928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32416750-C-G

128729938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32416740-T-C

128730353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32416361-C-T

128730567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32416147-T-C

128730741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32415971-G-A

http://identifiers.org/hco/11/GRCh38#128730946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32415769-A-C

128731407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32415322-T-A

http://identifiers.org/hco/11/GRCh38#128731605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32415183-C-A

128731630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32415159-G-A

128731652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32415137-T-C

128731794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32414992-G-A

128732439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32414386-C-T

128732521-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32414334-G-C

128732579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32414234-T-C

128732642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32414191-T-C

128733139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413731-G-A

128733139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413731-G-T

128733269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413601-G-A

128733269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413601-G-T

128733417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413468-C-T

128733420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32413465-A-G

128733940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32412887-C-T

128734894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32412080-G-A

128734953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32412022-G-A

128735152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411760-G-A

128735334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411597-A-G

128735432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411505-G-A

128735492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411446-A-G

128736059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411021-T-C

128736068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32411012-A-G

http://identifiers.org/hco/11/GRCh38#128736162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32410914-C-A

128736162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410914-C-G

128736162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410914-C-T

128736195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410879-T-A

128736195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410879-T-C

128736260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410814-T-G

128736371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32410716-G-A

128736420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410679-T-A

128736687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410358-T-C

128736954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32410110-G-A

http://identifiers.org/hco/11/GRCh38#128737091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32409985-C-A

128737171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32409904-G-A

128737664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32408655-C-T

128737809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32408514-T-A

128737850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32408468-C-T

128738051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32408177-C-T

128738163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32408055-A-G

128738299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407950-T-C

128738570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407697-T-C

128739043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407190-G-A

128739043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407190-G-C

128739106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407128-C-G

128739106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407128-C-T

128739232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32407006-C-T

128739296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406942-T-A

http://identifiers.org/hco/11/GRCh38#128739420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32406852-C-A

128739590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406709-G-A

128739590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406709-G-T

128739662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406635-A-T

128739669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406626-A-G

128739949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406347-C-T

128739950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406346-C-T

http://identifiers.org/hco/11/GRCh38#128739959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32406337-C-A

128739959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406337-C-T

128740143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32406170-G-A

128740754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32405270-T-C

128743067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: -G-C

128743539-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32403411-A-T

128743746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32403206-G-A

128743781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32403171-C-T

128744059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402890-G-A

128744108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402839-G-A

128744333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402597-C-T

128744551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402343-C-T

128744593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402301-T-C

128744600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402294-C-G

128744657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402238-G-A

128744671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402218-C-T

128744717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402169-A-G

128744873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32402045-A-G

128744937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401968-G-A

128744954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401951-C-G

128744954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401951-C-T

128744955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401950-T-C

128745084-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401812-A-T

128745087-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401807-A-T

128745175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401710-G-C

128745629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401255-C-G

128745629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401255-C-T

128745630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401254-C-G

http://identifiers.org/hco/11/GRCh38#128745751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32401127-C-A

128745751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401127-C-G

128745751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32401127-C-T

128745892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32400793-C-T

128745913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32400772-C-T

http://identifiers.org/hco/11/GRCh38#128746117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32400534-C-A

128746262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32400370-A-T

128746345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32400293-A-G

128747983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398835-T-C

128748041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398774-G-A

128748099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398719-G-T

128748102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398716-T-A

128748102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398716-T-C

128748102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398716-T-G

128748130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398689-A-G

128748130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398689-A-T

128748135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398684-G-T

128748166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398652-T-C

128748166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398652-T-G

128748206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398617-G-A

128748206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398617-G-C

128748220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398598-G-A

http://identifiers.org/hco/11/GRCh38#128748221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32398597-C-A

128748221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398597-C-T

128748225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398593-T-C

128748251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32398567-G-A

128748251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 32398567-G-T

http://identifiers.org/hco/11/GRCh38#128748633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32398178-C-A

128748773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32398020-A-G

128749635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32396255-T-C

128749920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32396061-T-C

128750017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395972-G-A

128750034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395955-C-T

128750424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395588-G-A

128750685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395368-C-G

128750762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395317-G-A

128750768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32395311-A-G

128751262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32393096-C-T

128751281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32393075-C-T

128751318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32393038-G-A

128751331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32393025-A-G

128752293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392993-C-T

128752431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392846-T-C

128752457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392820-G-T

128752478-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392798-A-G

128752892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392386-C-T

128752908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392370-A-G

128753149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392133-A-G

128753284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32392005-A-G

128753533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391810-G-T

128753568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391776-A-T

http://identifiers.org/hco/11/GRCh38#128753570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32391774-C-A

128753619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391724-T-C

http://identifiers.org/hco/11/GRCh38#128753726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32391625-C-A

128753804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391471-C-T

128753805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391470-G-A

128753880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391395-A-G

128754204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32391099-T-C

http://identifiers.org/hco/11/GRCh38#128754322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32390955-C-A

128754789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390651-G-A

128754797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390640-G-A

128754940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390489-A-G

128754944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390485-G-A

128754944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390485-G-T

128755068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32390373-T-C

128755676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389831-A-G

128756395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389388-C-T

128756524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389255-C-T

128756525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389254-A-G

128756547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389231-G-A

128756706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32389076-T-C

128756868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32388906-T-G

128757304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32388839-T-C

128757538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32388581-C-T

128757619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32388505-T-C

128757641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32388487-C-T

http://identifiers.org/hco/11/GRCh38#128757823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32388324-C-A

128758030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32388152-G-A

128758030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32388152-G-T

http://identifiers.org/hco/11/GRCh38#128758043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32388139-C-A

128758139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32388043-G-A

128758139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32388043-G-C

128758139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32388043-G-T

128758193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32387989-G-A

128758253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32387929-C-T

http://identifiers.org/hco/11/GRCh38#128758316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32387866-A-C

128758413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387825-G-A

128758413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387825-G-T

128758416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387822-G-A

128758416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387822-G-T

128758444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387816-A-G

http://identifiers.org/hco/11/GRCh38#128758458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32387801-C-A

128758458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387801-C-T

128758520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387790-C-G

128758914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387421-C-G

128759031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387311-T-C

128759078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387282-C-T

http://identifiers.org/hco/11/GRCh38#128759092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32387268-C-A

128759092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387268-C-G

128759107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32387253-G-A

128759589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32386805-G-C

http://identifiers.org/hco/11/GRCh38#128759625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32386786-A-C

128759987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32386442-C-T

128759988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32386441-A-G

128760141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386305-G-C

128760158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386280-G-T

128760322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386158-T-C

128760322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386158-T-G

128760394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386098-C-T

http://identifiers.org/hco/11/GRCh38#128760454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32386040-A-C

128760485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32386007-C-T

128761138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385714-C-T

128761346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385527-T-C

128761401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385479-G-A

128761403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385477-G-T

128761419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385456-G-A

128761457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32385418-A-G

128761808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32384810-C-G

128761808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32384810-C-T

http://identifiers.org/hco/11/GRCh38#128762201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32384121-C-A

128762744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32382293-G-T

128762746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32382292-C-T

128763034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32382091-C-T

128763513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381614-T-C

128763841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381384-C-T

128763914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381325-C-T

128764068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381178-G-A

128764218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381084-C-T

128764271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32381034-C-G

http://identifiers.org/hco/11/GRCh38#128764531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32380804-C-A

128764531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380804-C-T

http://identifiers.org/hco/11/GRCh38#128764542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32380793-C-A

128764550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380785-G-A

128764550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380785-G-T

128764699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380622-G-A

128764895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380460-G-A

http://identifiers.org/hco/11/GRCh38#128764928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32380427-C-A

128764928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380427-C-T

128764948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380406-T-C

128764982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380364-A-G

http://identifiers.org/hco/11/GRCh38#128764985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32380361-A-C

128765036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380335-T-G

128765190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32380208-T-C

http://identifiers.org/hco/11/GRCh38#128765324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32380074-C-A

http://identifiers.org/hco/11/GRCh38#128765411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32379990-A-C

128765477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379926-G-A

128765477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379926-G-T

http://identifiers.org/hco/11/GRCh38#128765530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32379874-C-A

128765742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379713-G-A

128765767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32379688-T-C

128765783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32379672-C-T

128765789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32379666-T-C

128765821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379624-T-A

128765821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379624-T-C

128765903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32379413-G-A

128766005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32379271-T-C

128766048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32379194-G-T

128766219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32378975-T-C

128766671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32378527-G-A

128766687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32378513-G-A

128767122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32378071-C-G

128767126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32378067-G-A

128767242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377955-T-A

128767242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377955-T-C

128767303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377842-C-T

128767538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377611-A-G

http://identifiers.org/hco/11/GRCh38#128767727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32377469-C-A

128767877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377312-G-T

128767930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32377280-G-A

128768300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32376952-G-A

128768300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32376952-G-T

128768313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32376939-C-T

128768425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32376922-T-A

128768425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32376922-T-C

128768571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376886-C-G

128768626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376866-T-A

128768626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376866-T-C

128768732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376832-T-C

128768743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376821-C-T

128769505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32376115-G-A

128769625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32375985-G-A

128769831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32375634-T-C

128769879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32375597-A-G

128770510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32375019-G-A

128770510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32375019-G-T

128770559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374970-A-T

128770625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374904-A-G

128770641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374887-G-A

128770686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374842-T-C

128770723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374794-G-A

128770760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374757-C-T

128770814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374717-C-G

128770814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374717-C-T

128770985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374526-G-A

128771060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374455-T-G

128771122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374415-A-G

128771143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374383-C-T

128771173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374354-C-T

128771669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374022-G-A

128771672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374020-G-A

128771678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32374014-G-A

128771830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373868-G-A

128772447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373249-C-T

128772507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373202-G-A

128772517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373192-C-T

128772553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373155-G-A

128772632-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373076-A-T

128772643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373065-G-A

128772643-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373065-G-C

128772643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373065-G-T

128772645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32373063-A-G

128772700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372908-A-G

128773046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372476-G-C

128773048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372474-G-A

128773053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372469-T-A

128773069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372455-G-A

128773069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372455-G-T

128773114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372411-T-C

128773140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372385-G-A

128773140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32372385-G-T

128773634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371940-G-A

128773634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371940-G-T

128773883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371734-T-G

128773933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371676-G-T

128774269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371342-G-C

128774309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371317-C-T

128774455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371168-T-A

128774563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32371051-G-A

128774896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32370681-G-C

http://identifiers.org/hco/11/GRCh38#128774925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32370652-C-A

128774974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32370586-G-A

128775533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32369220-G-A

128775918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368873-G-T

128775937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368852-T-C

128776611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368240-A-G

128776611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368240-A-T

128776707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368149-C-G

128776745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32368112-T-C

128776849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367999-A-G

128776925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367874-C-G

128776925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367874-C-T

128776950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367850-A-G

128776958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367842-A-G

128777014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367787-A-G

128777187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367610-C-T

128777402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367382-G-A

128777403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367381-C-T

128777564-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367223-T-G

128777630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367159-T-C

128777635-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367154-C-G

http://identifiers.org/hco/11/GRCh38#128777661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32367129-A-C

128777669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32367123-C-T

128777834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32366956-G-A

128777861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32366929-C-T

128777912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32366890-T-C

128777914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32366888-T-C

128777959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32366846-C-T

128778846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32365339-A-G

128778866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32365318-G-A

128778876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32365302-C-T

128779323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364858-C-T

128779494-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364682-T-A

128780116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364438-T-G

128780171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364407-A-T

128780219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364364-A-G

http://identifiers.org/hco/11/GRCh38#128780807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32364084-C-A

128780807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364084-C-T

128780867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32364022-G-T

128781021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363867-G-C

128781021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363867-G-T

128782042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363408-G-A

128782042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363408-G-T

http://identifiers.org/hco/11/GRCh38#128782069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32363383-C-A

http://identifiers.org/hco/11/GRCh38#128782070-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32363382-A-C

128782088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363364-G-A

128782088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363364-G-C

128782100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363352-G-A

128782100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363352-G-T

http://identifiers.org/hco/11/GRCh38#128782101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32363351-C-A

128782101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363351-C-T

128782114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363337-T-G

128782118-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363329-T-A

http://identifiers.org/hco/11/GRCh38#128782124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32363323-A-C

128782124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363323-A-G

128782124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363323-A-T

http://identifiers.org/hco/11/GRCh38#128782271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32363099-A-C

128782275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32363095-T-C

128782691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362975-C-G

128782705-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362959-A-T

128782741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362924-T-C

128783524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362336-C-T

128783610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362266-G-A

128783656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362226-G-A

128783942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32362047-G-A

128784169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361862-A-G

128784303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361762-G-A

128784380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361685-T-C

128784444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32361625-C-G

128784444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 32361625-C-T

128784696-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361389-C-G

128785001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361100-C-T

128785014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32361087-A-G

128785114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32360979-A-G

128785161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32360947-T-C

128785276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32360836-T-C

128785528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359929-T-A

128785700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359784-T-C

128785747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359737-A-T

128785762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359720-T-C

128785885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359613-T-C

http://identifiers.org/hco/11/GRCh38#128785947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32359552-A-C

http://identifiers.org/hco/11/GRCh38#128785984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32359514-A-C

128785987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359511-G-A

128786008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359498-T-C

128786071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359446-A-G

128786100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359416-G-T

128786258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359295-G-A

128786327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359236-A-G

128786350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359216-G-A

128786559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32359041-T-C

128786611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358996-G-A

128786706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358887-C-G

128786709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358884-A-G

128786710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358883-C-T

128786787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358811-C-T

128786885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358716-G-A

128786994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358590-A-G

128787301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358307-C-G

128787318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32358290-A-G

http://identifiers.org/hco/11/GRCh38#128787322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32358286-C-A

128787678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32357509-A-G

128787695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32357492-C-T

128788754-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356761-A-T

128788910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356618-G-A

128788910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356618-G-T

128788996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356576-T-C

128789249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356319-A-G

128789249-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356319-A-T

http://identifiers.org/hco/11/GRCh38#128789365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32356233-C-A

128789366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356232-G-A

128789444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32356157-C-T

128789742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355885-C-G

128790231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355573-C-G

128790273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355509-G-A

128790273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355509-G-T

128790280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355502-A-G

128790280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355502-A-T

128790287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355495-G-C

128790287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355495-G-T

128790302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355480-A-T

128790308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355474-A-T

128790714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32355081-C-T

128790930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32354871-G-C

128790953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32354856-G-A

128791273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32354631-T-C

128791413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32354542-A-G

http://identifiers.org/hco/11/GRCh38#128791660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32354301-C-A

128791703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32354227-C-G

128792060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32353759-T-C

128792302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32353208-T-C

128792331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32353178-T-C

128793361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352839-G-A

128793371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352829-A-G

http://identifiers.org/hco/11/GRCh38#128793677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32352528-A-C

128793702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352503-T-C

128793797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352404-C-T

128793924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352287-C-T

128793990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352218-C-T

128794100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352123-C-T

128794134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352090-G-A

128794141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352083-C-T

128794148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32352076-T-G

128794270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32351956-A-G

128794340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32351878-C-T

128795433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32350598-A-G

128795433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32350598-A-T

128795868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32349833-T-A

128796128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32349607-C-T

128796335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32349434-T-C

128796335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32349434-T-G

128797004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32349114-A-T

128797421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32348760-T-C

http://identifiers.org/hco/11/GRCh38#128797501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32348680-A-C

128797813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32348372-C-T

128798047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32348168-G-A

128798272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347967-T-G

128798368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347876-G-A

128798642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347600-T-G

128798667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347570-T-C

128798845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347392-T-C

http://identifiers.org/hco/11/GRCh38#128798929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32347341-C-A

128799473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32347058-A-G

128799750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32346758-T-G

128799969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32346556-C-G

128800329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32346411-C-T

128800426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32346316-A-G

128800595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32346171-A-G

128800800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345983-T-G

128800925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345862-T-C

128801070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345715-G-A

128801079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345706-A-G

128801223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345546-G-A

128801346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345444-T-C

128801496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32345155-G-C

128802046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344693-G-A

128802121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344609-G-A

128802121-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344609-G-C

128802130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344600-G-A

128802130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344600-G-T

128802289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344461-G-A

128802428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344329-A-G

128802529-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344239-T-G

128802622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32344144-G-T

http://identifiers.org/hco/11/GRCh38#128802789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32343984-A-C

128803187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32343371-C-T

128803241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32343312-C-T

128803331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32343221-G-A

128803609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32342953-C-T

http://identifiers.org/hco/11/GRCh38#128803714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32342858-A-C

128803850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 32342706-A-G

http://identifiers.org/hco/11/GRCh38#128803996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32342585-C-A

http://identifiers.org/hco/11/GRCh38#128803997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32342584-C-A

128803997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32342584-C-T

http://identifiers.org/hco/11/GRCh38#128804184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32342375-C-A

http://identifiers.org/hco/11/GRCh38#128804197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32342362-C-A

128804443-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32342116-G-T

http://identifiers.org/hco/11/GRCh38#128804761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341855-C-A

128804761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32341855-C-T

128804764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32341852-G-A

128804764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32341852-G-C

http://identifiers.org/hco/11/GRCh38#128804774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341842-C-A

128804774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32341842-C-T

128804810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32341805-A-G

128804837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341778-G-A

128804837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341778-G-T

128804964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341655-G-A

128804964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341655-G-T

128805012-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341610-T-G

128805079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341545-A-G

128805086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341538-A-G

128805086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341538-A-T

128805110-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341514-A-T

128805202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341430-A-G

http://identifiers.org/hco/11/GRCh38#128805214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341422-C-A

128805222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341415-G-T

http://identifiers.org/hco/11/GRCh38#128805309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341323-C-A

128805339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341293-G-A

128805339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341293-G-T

http://identifiers.org/hco/11/GRCh38#128805345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341287-C-A

128805345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341287-C-G

128805345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341287-C-T

http://identifiers.org/hco/11/GRCh38#128805425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32341208-A-C

128805425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32341208-A-G

128805455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341181-T-C

128805490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341134-G-A

128805490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341134-G-T

128805514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341110-A-G

128805538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341086-T-G

128805592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341045-G-T

128805605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341032-G-A

128805605-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341032-G-C

128805605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341032-G-T

128805610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32341027-G-T

128805686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340947-G-A

128805686-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340947-G-C

128805711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340922-G-T

128805794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340846-A-G

http://identifiers.org/hco/11/GRCh38#128805798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340842-C-A

128805798-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340842-C-G

128805798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340842-C-T

128805806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340834-T-C

http://identifiers.org/hco/11/GRCh38#128805811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340829-C-A

128805872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340810-T-C

128805936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340782-G-A

128806000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340719-A-G

http://identifiers.org/hco/11/GRCh38#128806004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340715-C-A

128806044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340680-T-C

128806106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340619-G-T

128806201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340534-C-T

http://identifiers.org/hco/11/GRCh38#128806257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340478-C-A

128806257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340478-C-T

128806316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340421-T-G

128806407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340308-G-T

http://identifiers.org/hco/11/GRCh38#128806446-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340275-C-A

128806477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340251-C-T

http://identifiers.org/hco/11/GRCh38#128806503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340228-C-A

128806503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340228-C-T

128806526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340205-A-G

128806531-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340200-T-A

128806531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340200-T-G

128806613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340145-A-G

http://identifiers.org/hco/11/GRCh38#128806632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340126-C-A

128806634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340124-A-G

128806698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340072-G-C

128806698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32340072-G-T

http://identifiers.org/hco/11/GRCh38#128806751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32340017-C-A

http://identifiers.org/hco/11/GRCh38#128807017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32339502-C-A

128807017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339502-C-T

128807026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339495-G-C

128807026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339495-G-T

128807081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339443-T-A

128807081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339443-T-G

128807097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339437-T-C

http://identifiers.org/hco/11/GRCh38#128807131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32339414-C-A

128807131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339414-C-G

128807131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339414-C-T

128807132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339413-T-C

128807135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339410-G-A

128807135-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339410-G-C

128807135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339410-G-T

128807138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339400-A-G

128807139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339399-G-A

128807139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339399-G-C

128807139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339399-G-T

http://identifiers.org/hco/11/GRCh38#128807147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32339391-C-A

128807147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 32339391-C-T

128807280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339259-A-G

128807282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339257-A-G

128807282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339257-A-T

http://identifiers.org/hco/11/GRCh38#128807332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32339118-C-A

128807332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339118-C-T

128807343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339107-T-A

128807343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32339107-T-C

128807381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338912-T-C

http://identifiers.org/hco/11/GRCh38#128807469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32338795-A-C

128807470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338794-A-G

128807575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338703-C-G

128807582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338697-A-G

128807607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338672-C-T

128807626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338657-A-G

128807633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338650-C-T

128807654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338637-T-C

128807783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338460-G-A

128807905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338348-C-T

128808201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338098-T-C

128808202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338097-G-T

128808477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32338004-T-C

128808807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337700-G-A

http://identifiers.org/hco/11/GRCh38#128808931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32337565-A-C

128809084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337464-G-A

128809084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337464-G-T

128809105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337443-T-C

128809243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337307-T-C

128809288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337255-A-G

128809303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337240-G-A

128809303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337240-G-T

128809393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32337165-T-C

128809685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336926-G-C

128809820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336780-A-G

128809905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336704-T-C

128809983-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336638-T-A

128809990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336631-G-A

128809990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336631-G-T

128810003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336617-A-G

128810020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336600-G-C

128810070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336535-A-G

128810146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32336454-G-T

http://identifiers.org/hco/11/GRCh38#128810434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32335622-C-A

128810434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32335622-C-G

128810434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32335622-C-T

128810506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32335552-G-A

128810506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32335552-G-T

http://identifiers.org/hco/11/GRCh38#128810773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32335285-C-A

128810773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32335285-C-G

128810773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32335285-C-T

128811108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334954-T-C

128811240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334819-A-G

128811592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334444-C-T

http://identifiers.org/hco/11/GRCh38#128811599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32334437-C-A

128811599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334437-C-T

http://identifiers.org/hco/11/GRCh38#128811610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32334426-C-A

128811610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334426-C-T

128811648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32334388-T-C

http://identifiers.org/hco/11/GRCh38#128811688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32334241-C-A

http://identifiers.org/hco/11/GRCh38#128812142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32333781-C-A

128812460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32333461-A-G

128812468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32333453-C-T

128812514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32333034-C-T

128812630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332929-G-A

128812630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332929-G-T

128812631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332928-G-A

128812698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332870-G-A

128812698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332870-G-T

http://identifiers.org/hco/11/GRCh38#128812709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32332857-C-A

http://identifiers.org/hco/11/GRCh38#128812792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32332794-A-C

128812792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332794-A-G

128812802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332784-T-C

128812836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332757-A-T

128812886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332706-G-T

128812907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332685-T-C

http://identifiers.org/hco/11/GRCh38#128812958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#32332642-C-A

128812958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332642-C-T

128813050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332528-A-G

128813071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332508-G-A

128813079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332500-G-A

128813128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332457-A-G

128813180-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3749
most severe consequence: 3 prime UTR variant
orthologous variants: 32332401-C-G