101745525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88283159-G-T

101745591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88283093-T-C

101745707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282996-T-C

101745752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282952-G-A

http://identifiers.org/hco/12/GRCh38#101745786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282897-C-A

101745839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282875-G-T

101745848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282866-A-G

http://identifiers.org/hco/12/GRCh38#101745917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282807-C-A

101745917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282807-C-T

101745950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282781-T-A

http://identifiers.org/hco/12/GRCh38#101745955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282776-C-A

101745955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282776-C-T

http://identifiers.org/hco/12/GRCh38#101746023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282710-C-A

101746023-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282710-C-G

101746023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282710-C-T

101746047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282689-A-G

101746220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282612-A-G

http://identifiers.org/hco/12/GRCh38#101746315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282530-A-C

101746361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282488-C-T

101746418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282433-A-G

101746478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282366-G-A

101746478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282366-G-C

101746478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282366-G-T

101746541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282304-T-C

http://identifiers.org/hco/12/GRCh38#101746692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282162-C-A

http://identifiers.org/hco/12/GRCh38#101746734-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282110-A-C

101746734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282110-A-G

101746734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282110-A-T

101746736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282108-T-C

101746766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282071-T-A

101746766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282071-T-C

http://identifiers.org/hco/12/GRCh38#101746768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282069-A-C

101746768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282069-A-G

http://identifiers.org/hco/12/GRCh38#101746793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88282044-C-A

101746803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282034-T-A

101746823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88282014-G-C

101746912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281944-G-T

101747010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281854-T-C

http://identifiers.org/hco/12/GRCh38#101747061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88281803-C-A

101747061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281803-C-T

101747063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281801-G-A

101747063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281801-G-T

101747071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281793-T-C

101747086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: 88281777-C-T

http://identifiers.org/hco/12/GRCh38#101747097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88281766-C-A

http://identifiers.org/hco/12/GRCh38#101747297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88281564-A-C

101747297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281564-A-T

101747299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281562-G-A

101747299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281562-G-T

101747307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281554-A-G

101747548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281325-A-G

101747577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88281293-T-A

101747965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88280445-C-T

101748031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88280399-G-C

101748466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88280012-A-G

101748473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88280007-T-C

101748523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279960-C-T

101748555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279931-T-C

101748834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279713-T-A

101748950-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279603-T-A

101748954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279599-A-T

101748997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88279470-A-G

101749183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 88279177-T-C

101749243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279157-C-T

http://identifiers.org/hco/12/GRCh38#101749244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88279156-A-C

101749244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279156-A-G

101749244-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279156-A-T

101749265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279134-T-C

101749286-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279116-G-C

101749286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279116-G-T

101749319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279083-T-C

http://identifiers.org/hco/12/GRCh38#101749328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88279074-C-A

http://identifiers.org/hco/12/GRCh38#101749330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88279072-C-A

101749330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88279072-C-T

101752832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276453-A-T

101753322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276300-C-T

101753363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276260-A-G

http://identifiers.org/hco/12/GRCh38#101753471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88276152-A-C

101753483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 88276140-A-G

http://identifiers.org/hco/12/GRCh38#101753558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88276065-A-C

101753575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276053-A-G

101753575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276053-A-T

101753591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276037-T-C

101753624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88276004-T-A

101753716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 88275915-C-T

http://identifiers.org/hco/12/GRCh38#101757003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88275648-C-A

101757021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275630-G-A

101757024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275627-C-T

101757025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275626-A-G

101757033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275620-G-A

101757085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275567-G-A

101757085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275567-G-T

101757096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275556-G-A

101757096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275556-G-C

101757096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275556-G-T

http://identifiers.org/hco/12/GRCh38#101757097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88275555-C-A

101757097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275555-C-T

http://identifiers.org/hco/12/GRCh38#101757101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88275547-C-A

101757101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275547-C-T

101757158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88275492-T-C

101757236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88275385-A-G

101757236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 88275385-A-T

101757368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275255-A-G

101757385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275238-A-G

101757403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275221-G-T

http://identifiers.org/hco/12/GRCh38#101757417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88275207-C-A

101757417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275207-C-T

101757475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275162-C-G

http://identifiers.org/hco/12/GRCh38#101757537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88275103-A-C

101757557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275088-G-A

101757557-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275088-G-C

101757557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275088-G-T

101757558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 88275087-C-T

101757659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88274986-T-A

101757659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 88274986-T-C

101757666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88274979-A-G

101757682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88274964-G-A

101757682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88274964-G-T

101759454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88273842-T-A

101759947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88273464-G-T

101759950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88273461-G-T

101759973-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88273439-T-A

101760018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88273420-C-T

101760067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88273371-A-G

101760165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88273276-A-G

101760165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88273276-A-T

101760257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272979-G-T

http://identifiers.org/hco/12/GRCh38#101760294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88272907-C-A

101760371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272834-C-G

101760419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272788-G-A

101761086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272475-A-T

101761092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272466-A-G

101761102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272456-A-T

101761115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272443-A-G

http://identifiers.org/hco/12/GRCh38#101761361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88272197-C-A

101761361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272197-C-T

101761439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272165-G-A

101761439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88272165-G-T

http://identifiers.org/hco/12/GRCh38#101761532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88272093-A-C

http://identifiers.org/hco/12/GRCh38#101761841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88271769-A-C

101761991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88271659-G-A

101762504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88271216-T-C

101763600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270441-T-C

101763848-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270241-T-A

101764055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270102-G-A

101764055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270102-G-T

101764087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270066-T-A

101764088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270065-T-C

101764088-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88270065-T-G

101764151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88269998-A-G

101764151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88269998-A-T

101764314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88269854-T-A

101764335-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, undefined
orthologous variants: 88269833-C-G

101764335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, undefined
orthologous variants: 88269833-C-T

101764431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88269758-T-C

101764441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88269748-T-C

101764442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: synonymous variant
orthologous variants: 88269747-G-A

101764601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: synonymous variant
orthologous variants: 88269609-T-C

101764636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88269574-T-C

101764636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88269574-T-G

http://identifiers.org/hco/12/GRCh38#101764791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88269422-A-C

101765344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88268870-G-T

101765564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88268776-T-C

101765662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88268676-G-A

101765662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88268676-G-C

101765662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88268676-G-T

101766080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88268515-A-G

101766132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88268463-T-C

http://identifiers.org/hco/12/GRCh38#101766268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88268327-C-A

101766271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88268324-T-C

101768007-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 88267341-T-A

101768197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88267156-G-A

101768218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88267142-T-C

101768218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88267142-T-G

101768240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88267127-A-G

101768375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88266994-T-C

101768569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88266804-T-C

http://identifiers.org/hco/12/GRCh38#101769530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: -A-C

101769544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: -G-C

101769934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265951-T-G

101769935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265950-A-G

http://identifiers.org/hco/12/GRCh38#101769999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88265887-C-A

101770310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265595-G-A

101770310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265595-G-T

101770388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265518-T-C

101770593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88265306-A-G

http://identifiers.org/hco/12/GRCh38#101770619-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88265281-A-C

101770619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88265281-A-G

101770855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264709-T-C

101770928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264635-A-G

101770928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264635-A-T

101770983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264523-G-A

101771434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264249-G-C

101771514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264192-G-A

101771526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88264178-G-A

101772570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88263593-T-A

101772742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88263445-C-G

http://identifiers.org/hco/12/GRCh38#101772747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88263440-C-A

http://identifiers.org/hco/12/GRCh38#101773758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#88262488-C-A

101773758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, undefined
orthologous variants: 88262488-C-T

101773804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88262443-G-A

101776117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88259301-A-G

101776136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88259282-T-C

101776136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88259282-T-G

http://identifiers.org/hco/12/GRCh38#101776147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88259271-A-C

101776245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88259181-T-G

http://identifiers.org/hco/12/GRCh38#101776414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88259018-A-C

101776425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88259007-G-A

101776826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258671-T-C

101776905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258593-G-A

101776905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258593-G-C

101777127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258434-C-T

101777139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258422-T-C

101777237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258333-G-A

101777320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88258275-C-T

101777445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257957-G-A

101777629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257732-C-T

101777678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257667-T-C

101777704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257631-T-G

101778151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257099-T-A

101778166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257085-T-C

http://identifiers.org/hco/12/GRCh38#101778213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88257036-C-A

101778213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257036-C-T

101778217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257032-G-A

101778224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257025-A-G

101778224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88257025-A-T

101778257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88256998-A-G

101778260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88256995-A-G

101778266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88256989-G-A

101778266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88256989-G-T

101778342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256919-T-C

101778354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256907-T-C

101778473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256790-A-G

101778576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256685-A-G

101778697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256515-A-G

101778704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256493-G-C

101778704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256493-G-T

101778890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256391-A-G

http://identifiers.org/hco/12/GRCh38#101778937-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88256362-A-C

101778958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256347-G-T

101779011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256297-T-C

101779083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256245-G-A

http://identifiers.org/hco/12/GRCh38#101779122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88256209-C-A

http://identifiers.org/hco/12/GRCh38#101779124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88256207-C-A

101779159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256184-T-C

http://identifiers.org/hco/12/GRCh38#101779171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88256175-C-A

101779326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256087-G-A

101779356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256058-C-G

101779379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88256036-A-G

101779443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255985-T-C

101779475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255957-C-T

http://identifiers.org/hco/12/GRCh38#101779521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88255918-C-A

101779598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255838-G-T

101779602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255834-A-T

http://identifiers.org/hco/12/GRCh38#101779608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88255828-C-A

101779608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255828-C-T

101779611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255825-G-A

http://identifiers.org/hco/12/GRCh38#101779615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88255821-C-A

101779619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255817-A-G

http://identifiers.org/hco/12/GRCh38#101779669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88255784-C-A

101779669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255784-C-T

101780052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255480-T-C

101780123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255445-G-A

101780123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255445-G-C

101780123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 88255445-G-T

101780254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: synonymous variant
orthologous variants: 88255318-T-C

101780264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88255308-C-T

101780372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88255202-T-G

101780574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88255032-C-T

101780612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88254994-G-A

101780612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense variant
orthologous variants: 88254994-G-T

http://identifiers.org/hco/12/GRCh38#101780644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88254962-C-A

101780644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254962-C-G

101780644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254962-C-T

101780659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254943-T-A

101780659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254943-T-C

http://identifiers.org/hco/12/GRCh38#101780662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88254940-A-C

101780662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254940-A-G

101780671-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254931-T-A

101780692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254910-G-A

101780692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254910-G-T

101780734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254867-T-C

101780734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254867-T-G

http://identifiers.org/hco/12/GRCh38#101780769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88254834-C-A

101780769-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254834-C-G

101780806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254797-G-A

101780902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254700-T-A

101781222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254425-C-T

http://identifiers.org/hco/12/GRCh38#101781292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88254359-C-A

101781543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254163-A-G

101781593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254115-G-A

101781593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88254115-G-C

101781836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88253922-A-G

101781985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88253751-G-A

101782001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88253735-C-T

http://identifiers.org/hco/12/GRCh38#101782057-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88253690-C-A

101782153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88253463-C-T

101782692-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88252929-T-A

http://identifiers.org/hco/12/GRCh38#101782880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88252753-C-A

101782906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88252731-C-T

101782922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88252716-T-A

http://identifiers.org/hco/12/GRCh38#101782923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88252715-C-A

101782977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88252681-C-T

101783102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88252570-C-T

101784487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251947-G-A

101784619-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251847-T-G

http://identifiers.org/hco/12/GRCh38#101784674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88251801-C-A

101784729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251751-A-G

101784867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251637-G-A

101784884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251620-C-T

101785223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251347-C-T

101785227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251343-T-C

101785285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88251299-C-T

http://identifiers.org/hco/12/GRCh38#101785962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88250512-C-A

101785962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88250512-C-G

101786004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88250469-G-C

101786004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88250469-G-T

101786005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 88250468-A-G

101786161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88250309-A-G

101786161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 88250309-A-T

101786247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88250238-T-C

http://identifiers.org/hco/12/GRCh38#101786351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88250148-C-A

101786561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88249771-G-A

101786824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88249594-A-G

101787878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88249174-A-G

101787963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88249085-T-C

101788024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88249036-G-A

101788153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248895-T-C

101788345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248724-G-A

101788384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248677-C-T

101788407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248657-A-T

101788429-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248637-T-A

101788429-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248637-T-C

101788463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248582-G-A

101788463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248582-G-T

101788464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248581-T-C

101788620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88248432-A-G

101789955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 88247878-C-T

http://identifiers.org/hco/12/GRCh38#101790019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88247814-C-A

101790062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88247771-G-A

101790062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 88247771-G-C

101790113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88247677-A-G

http://identifiers.org/hco/12/GRCh38#101792085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88243892-A-C

101792707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88243281-G-A

101792839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88243140-C-T

101793078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88242824-A-G

101793114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron variant
orthologous variants: 88242788-C-T

101793610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, undefined
orthologous variants: 88241831-T-C

http://identifiers.org/hco/12/GRCh38#101795994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88237840-C-A

101795994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88237840-C-T

101796067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88237792-T-C

101796071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88237788-T-C

101796097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88237764-A-G

101796137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 88237722-T-C

101796262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 88237623-C-T

101796788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236482-T-A

101796788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236482-T-C

101796788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236482-T-G

101796789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236481-C-G

101796809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236461-G-A

101796809-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236461-G-C

101796809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236461-G-T

101796862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88236408-A-G

101797550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235895-G-A

101797695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235772-G-A

101798032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235491-C-G

101798032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235491-C-T

101798101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235428-T-C

101798147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88235383-A-G

101819406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88229096-C-T

101819650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228600-T-C

http://identifiers.org/hco/12/GRCh38#101819828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88228413-C-A

101819828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228413-C-T

101819889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228349-T-C

101819922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228318-T-C

101820015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228232-G-A

101820101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228145-C-T

101820186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88228053-G-A

101821246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88226247-G-A

101821557-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225941-A-T

101821579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225919-T-C

101821664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225842-G-A

101822683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225195-G-T

101822767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225111-A-G

101822795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88225081-G-A

101822923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88224954-T-C

101822923-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88224954-T-G

101824073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 88222387-C-T

101824158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88222294-C-T

101824289-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88222177-A-T

101825025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221846-C-T

101825055-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221817-G-C

101825121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221758-T-C

101825176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221700-A-G

101825178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221698-A-G

101825184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221694-G-T

101825645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221283-A-G

101825645-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221283-A-T

101825757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221018-T-C

101825763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88221012-G-A

101825948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220690-C-T

101825988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220630-G-A

101826116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220514-A-T

101826262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220369-G-A

101826442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220207-G-A

101826662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88220047-T-C

101827432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88219085-T-A

http://identifiers.org/hco/12/GRCh38#101827488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88219027-A-C

101828090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88218306-T-A

101828266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88218153-G-C

101828609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88217826-G-T

http://identifiers.org/hco/12/GRCh38#101828703-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88217705-A-C

101828999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88217397-C-T

101829241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88217254-T-C

http://identifiers.org/hco/12/GRCh38#101829298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88217209-A-C

101829311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88217197-T-C

http://identifiers.org/hco/12/GRCh38#101829455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88217070-A-C

101829661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88216914-A-G

101829688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88216886-A-G

101829885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88216693-A-G

101829914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88216665-C-T

http://identifiers.org/hco/12/GRCh38#101829967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88216614-A-C

101830066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88216533-T-C

101830508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88215437-G-A

101830508-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88215437-G-C

101830508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88215437-G-T

101830512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 88215433-A-G

http://identifiers.org/hco/12/GRCh38#101830699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88215255-C-A

101830699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215255-C-T

101830732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215232-G-A

101830732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215232-G-T

http://identifiers.org/hco/12/GRCh38#101830791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88215172-C-A

http://identifiers.org/hco/12/GRCh38#101830807-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#88215156-A-C

101830925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215037-C-T

101830933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215029-G-A

101830933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215029-G-C

101830943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215019-G-A

101830943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215019-G-T

101830949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215014-G-A

101830949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29670
most severe consequence: 5 prime UTR variant
orthologous variants: 88215014-G-C