124044458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58470975-C-T

124044618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58471144-G-T

http://identifiers.org/hco/8/GRCh38#124044623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58471149-A-C

124044998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58471511-T-C

http://identifiers.org/hco/8/GRCh38#124045121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58471668-A-C

124045183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58471703-C-T

124045354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58471847-A-T

124045438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58471929-A-G

124045886-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58472280-T-A

124045898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58472292-T-C

http://identifiers.org/hco/8/GRCh38#124046012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58472401-C-A

124046012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472401-C-T

124046020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472409-G-A

124046021-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472410-T-A

124046021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472410-T-C

124046025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472414-T-A

124046025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472414-T-C

124046076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472454-G-T

124046212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472582-G-T

124046214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472584-A-G

124046221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472591-C-T

124046316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472681-A-G

124046324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472689-G-A

124046324-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472689-G-C

124046324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472689-G-T

124046335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472706-G-A

124046335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472706-G-T

http://identifiers.org/hco/8/GRCh38#124046355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58472723-C-A

124046355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472723-C-G

124046355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472723-C-T

http://identifiers.org/hco/8/GRCh38#124046371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58472740-C-A

124046371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472740-C-T

124046445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472808-A-G

124046558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472920-G-A

124046565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58472928-T-C

http://identifiers.org/hco/8/GRCh38#124046756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58473094-A-C

124046763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58473109-T-C

124046775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58473121-T-C

124046934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473253-C-T

124046982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473299-G-A

http://identifiers.org/hco/8/GRCh38#124047066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58473381-A-C

124047066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473381-A-G

http://identifiers.org/hco/8/GRCh38#124047082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58473416-C-A

124047082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473416-C-T

124048832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473666-G-A

124048940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473763-G-T

124049002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473798-G-A

124049500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473916-G-A

124049542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473953-T-C

124049551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58473962-T-G

http://identifiers.org/hco/8/GRCh38#124049696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58474095-C-A

124049696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58474095-C-T

124049825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474228-T-C

124049848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474250-T-C

http://identifiers.org/hco/8/GRCh38#124049861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58474263-C-A

124049861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474263-C-T

http://identifiers.org/hco/8/GRCh38#124049867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58474269-C-A

http://identifiers.org/hco/8/GRCh38#124049892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58474297-C-A

124049892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474297-C-T

124049899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474304-G-A

124049899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474304-G-C

124049916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474322-A-G

124049933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474339-C-T

124050316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474719-G-A

124050337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474739-G-C

124050348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474771-A-G

124050413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58474980-G-A

http://identifiers.org/hco/8/GRCh38#124050505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58475152-A-C

124050514-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475161-C-G

124050621-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475307-G-C

124050631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475311-G-T

124050686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475371-G-A

124050710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475400-C-G

124050786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475488-G-A

124050786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475488-G-T

http://identifiers.org/hco/8/GRCh38#124050886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58475567-C-A

124050886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475567-C-T

124050890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475571-T-C

124050929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475600-A-G

124051035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475690-A-G

124051079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475734-T-A

124051645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475943-G-A

124051645-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58475943-G-C

124051788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476083-C-G

124051847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476142-G-A

124051967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476246-G-A

124051994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476272-C-T

124052209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58476516-C-T

http://identifiers.org/hco/8/GRCh38#124053155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58477430-A-C

124053955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58477899-C-T

http://identifiers.org/hco/8/GRCh38#124053963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58477908-C-A

124054067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478010-T-A

124054302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478202-G-A

124054512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58478396-T-A

124056484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58485895-G-A

124057221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

124058100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58487637-A-G

124058132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58487668-C-T

124058706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488566-G-A

124058734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488538-T-C

http://identifiers.org/hco/8/GRCh38#124058754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58488518-C-A

124058754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488518-C-G

124058760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488512-G-T

http://identifiers.org/hco/8/GRCh38#124058771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58488501-C-A

124058771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488501-C-T

124058824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488471-T-C

124058863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488439-T-C

124058866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488436-A-G

124058923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488380-C-G

124058968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488336-T-C

124059143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488163-A-G

124059267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58488079-A-G

124059626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58489844-G-A

http://identifiers.org/hco/8/GRCh38#124059709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58489914-C-A

124059750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58489930-G-A

http://identifiers.org/hco/8/GRCh38#124059832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58490010-A-C

124060127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490269-T-C

http://identifiers.org/hco/8/GRCh38#124060174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58490318-C-A

124060174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58490318-C-T

124060224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58490368-A-G

124060284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58490428-A-G

124060319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490469-T-A

124060319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490469-T-C

124060322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490472-T-C

http://identifiers.org/hco/8/GRCh38#124060442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58490588-C-A

124060442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490588-C-T

http://identifiers.org/hco/8/GRCh38#124060470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58490620-C-A

124060470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58490620-C-T

124060649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 58490777-C-T

124060821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58490975-G-C

124060821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58490975-G-T

http://identifiers.org/hco/8/GRCh38#124060831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58490985-C-A

124060886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491026-G-A

124060886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491026-G-T

124060914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491055-T-A

124060914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491055-T-C

124060915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491056-T-A

124060928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491069-C-T

124061117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491493-G-A

http://identifiers.org/hco/8/GRCh38#124061164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58491539-A-C

124061164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491539-A-T

http://identifiers.org/hco/8/GRCh38#124061297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58491648-A-C

124061337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58491688-C-T

http://identifiers.org/hco/8/GRCh38#124061401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58491747-C-A

124061697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492062-G-A

124061727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492091-G-A

124061727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492091-G-T

124061754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492117-G-A

124061754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492117-G-T

124061786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492148-G-A

http://identifiers.org/hco/8/GRCh38#124061804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58492175-C-A

124061869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492243-G-A

124061881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492255-G-A

124061881-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492255-G-C

124061881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492255-G-T

124061986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492360-G-A

124061987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492361-C-T

124062010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492384-G-A

124062014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58492388-G-A

124062136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492503-G-A

124062137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492504-G-A

124062178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492535-T-A

124062178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492535-T-C

124062195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492557-C-T

124062312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58492681-G-A

http://identifiers.org/hco/8/GRCh38#124062346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58492716-C-A

124062848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493307-C-G

124062875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493334-C-T

124062964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493428-G-A

124062987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493456-G-A

124063004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493474-C-T

http://identifiers.org/hco/8/GRCh38#124063042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58493495-C-A

124063042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493495-C-T

http://identifiers.org/hco/8/GRCh38#124063749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58493604-C-A

124063821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493671-T-C

124063973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58493823-G-T

124064198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494033-G-T

124064203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494038-T-C

124064203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494038-T-G

124064247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494083-G-A

124064269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494105-G-A

124064381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58494177-T-C

124064382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58494178-G-A

http://identifiers.org/hco/8/GRCh38#124064602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58494400-C-A

124064697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494497-T-C

124064732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58494531-T-C

124065446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495103-C-T

124065625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495259-G-C

124065823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495441-G-A

124065823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495441-G-T

124065856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495471-C-T

124065865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495488-C-T

124066099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495730-A-G

124066113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495744-T-A

124066175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495811-C-T

124066307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495944-T-A

124066307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58495944-T-C

124066565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497130-A-G

124066565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497130-A-T

124066583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497148-A-G

124066845-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497194-G-C

124066849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497198-G-C

http://identifiers.org/hco/8/GRCh38#124066914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58497246-C-A

124067008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497336-A-G

124067115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497444-G-T

124067427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497758-T-C

124067548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497859-C-T

124067555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497866-G-A

124067555-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497866-G-C

http://identifiers.org/hco/8/GRCh38#124067619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58497932-C-A

124067619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497932-C-T

124067628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497941-T-A

124067628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58497941-T-G

124067693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498004-G-T

http://identifiers.org/hco/8/GRCh38#124067726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58498049-C-A

124067726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498049-C-G

http://identifiers.org/hco/8/GRCh38#124067834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58498154-C-A

124067834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498154-C-G

124067850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498170-T-C

124068394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498882-T-C

124068401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498889-C-G

124068442-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58498930-C-G

124069376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58499369-G-A

124069376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58499369-G-C

124069397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58499390-T-C

http://identifiers.org/hco/8/GRCh38#124069469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58499471-C-A

124069508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499504-T-C

http://identifiers.org/hco/8/GRCh38#124069525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58499521-C-A

124069525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499521-C-T

124069563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499559-T-A

124069563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499559-T-G

124069585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499588-T-C

124069642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499642-A-G

124069697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499698-A-G

124069769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58499758-C-T

http://identifiers.org/hco/8/GRCh38#124070034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58500027-C-A

124070086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58500079-C-T

124070653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501348-T-C

124070659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501354-T-G

124070710-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501399-A-T

124070721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501410-A-G

124070732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501421-T-A

124070732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501421-T-C

124070834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58501829-C-T

124071242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502218-G-A

124071242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502218-G-C

124071270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502245-A-G

124071278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502252-G-A

124071286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502260-G-T

124071341-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502314-G-C

124071357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502330-G-A

124071357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502330-G-T

http://identifiers.org/hco/8/GRCh38#124071544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58502517-C-A

124071544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 58502517-C-T

124071656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502629-G-A

124071732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502698-T-C

124071746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502712-G-T

http://identifiers.org/hco/8/GRCh38#124071747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58502713-A-C

124071757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502723-G-C

124071757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502723-G-T

124071778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502744-A-G

124071902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502857-C-T

124072080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58502949-C-T

124072144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503009-G-A

http://identifiers.org/hco/8/GRCh38#124072194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58503073-C-A

124072216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503095-T-C

124072553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503439-A-G

124072673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503633-C-T

124072723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503674-G-A

124073055-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58503985-A-T

124073078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504008-C-T

124073308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 58504126-G-A

124073446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504274-G-C

124073475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504304-A-G

124073747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504580-T-C

124073883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504724-T-C

http://identifiers.org/hco/8/GRCh38#124073892-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58504733-A-C

124073895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504736-A-T

124074016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58504851-G-A

124074339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505172-T-A

124075851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505204-C-T

http://identifiers.org/hco/8/GRCh38#124075956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58505300-C-A

124076164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505477-A-G

http://identifiers.org/hco/8/GRCh38#124076282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58505595-C-A

124076282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58505595-C-G

124076282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58505595-C-T

http://identifiers.org/hco/8/GRCh38#124076415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58505785-C-A

124076415-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505785-C-G

124076415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505785-C-T

124076426-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505796-T-G

124076498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505868-T-C

124076534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505892-T-C

124076681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58505962-T-C

124076735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58506011-G-A

124076735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58506011-G-C

124077188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58506736-G-A

124077457-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58506965-T-G

124077490-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58506999-G-C

124077614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58507125-G-A

124077724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58507209-C-T

124078046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58507339-C-T

124078108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58507393-T-C

124078157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58507442-G-A

124079835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58508208-G-C

124079998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58508352-C-T

124080206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58508528-T-C

124080274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58508597-T-A

124080764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58508776-G-C

124080820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58508836-C-T

124081547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509173-A-G

124081828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509404-C-T

http://identifiers.org/hco/8/GRCh38#124082156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58509647-C-A

124082156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509647-C-T

124082177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509670-G-A

124082177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509670-G-C

124082177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509670-G-T

124082185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509675-A-T

124082230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509720-A-T

http://identifiers.org/hco/8/GRCh38#124082282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58509767-C-A

124082299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58509783-T-C

124082299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58509783-T-G

124082336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58509820-C-T

124082375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58509859-T-C

124082477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509959-G-A

124082477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509959-G-C

124082504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509985-G-C

124082504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58509985-G-T

124082528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58510010-G-A

124082528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58510010-G-T

124082756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58510161-G-A

124082817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58510229-A-G

http://identifiers.org/hco/8/GRCh38#124090727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58510990-C-A

124090880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511154-C-T

124090949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511215-T-C

124090989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511255-T-G

http://identifiers.org/hco/8/GRCh38#124091115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58511378-C-A

124091115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511378-C-T

http://identifiers.org/hco/8/GRCh38#124091248-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58511719-C-A

124091295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511780-G-T

124091357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511837-G-A

124091357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511837-G-T

124091385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511866-G-A

124091400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58511881-T-C

124091450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58511965-G-A

124091450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58511965-G-T

124091561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58512076-T-A

124091596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512111-A-G

124091644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512166-G-T

http://identifiers.org/hco/8/GRCh38#124092457-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58512405-C-A

124093520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512707-C-T

124093564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512766-A-G

124093601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512801-A-G

http://identifiers.org/hco/8/GRCh38#124093627-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58512827-A-C

124093663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512873-G-C

124093691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58512925-A-T

124093775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513005-C-T

124093891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513058-C-G

124093891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513058-C-T

124094211-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513290-G-C

124094265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513325-T-C

124094289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513343-T-G

124094386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513483-A-G

124094415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513509-T-C

124094777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513617-G-A

124094777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513617-G-T

124094804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513640-A-T

124094877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58513652-T-C

124095127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58514478-T-C

http://identifiers.org/hco/8/GRCh38#124095147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58514498-C-A

124097176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515157-C-G

124097187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515168-A-T

124097201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515182-T-C

http://identifiers.org/hco/8/GRCh38#124097450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58515422-C-A

124097566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515519-A-T

124097584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515537-T-C

124097764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515690-T-C

124097764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515690-T-G

124097815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58515741-T-A

124097815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58515741-T-C

124097851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58515777-A-G

http://identifiers.org/hco/8/GRCh38#124097908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58515834-C-A

124097908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515834-C-T

124097914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515838-T-G

124097944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515868-A-G

124097968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515891-A-T

http://identifiers.org/hco/8/GRCh38#124097980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58515901-C-A

124097980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515901-C-T

124098023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515950-T-A

124098023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58515950-T-C

124098160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58516665-A-T

124098218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58516725-T-G

124100352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518136-G-A

124100508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518294-G-A

124100529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518315-G-C

http://identifiers.org/hco/8/GRCh38#124100815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58518556-C-A

124100815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518556-C-T

124100838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518570-T-C

124100955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518645-G-A

124100955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518645-G-T

http://identifiers.org/hco/8/GRCh38#124100999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58518683-C-A

124100999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518683-C-T

124101005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518689-G-T

124101034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58518727-T-G

124101127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58518795-G-A

124101426-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58519095-T-A

124102725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520128-G-A

124102984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520339-T-C

http://identifiers.org/hco/8/GRCh38#124103020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58520376-C-A

124103037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520393-G-A

124103037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520393-G-T

124103134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520468-A-G

124103327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520661-G-A

124103341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520671-G-A

124103350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520680-T-G

124103493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58520871-T-C

124104053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58521327-G-A

124104107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58521362-T-C

124104243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58521513-G-T

124104271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58521551-G-C

124109659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523424-G-A

124109689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523456-C-G

124109727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523497-C-G

124109874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523662-C-T

124109885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523673-T-C

124110042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523864-C-T

124110052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58523869-G-A

124110193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58524043-C-G

124110236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58524086-T-C

http://identifiers.org/hco/8/GRCh38#124110263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58524113-C-A

124110263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58524113-C-T

124112383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526475-A-T

124112401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526492-C-T

124112628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526698-C-T

124112781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526830-T-C

124112823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526872-A-G

124112959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58526999-A-G

124113695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527347-T-A

124113696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527348-A-T

124113722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527374-C-G

124113763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527414-C-T

124113776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527427-G-A

124113831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527498-G-T

124113902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527547-G-A

124113916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527560-G-A

124113942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527585-G-A

124114154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58527948-T-C

124114272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58528054-C-G

124114677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58528389-T-C

124114950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58528819-A-T

124115121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529009-T-C

http://identifiers.org/hco/8/GRCh38#124115217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58529117-C-A

124115346-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529255-C-G

124115356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529265-G-A

124115356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529265-G-C

124115356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529265-G-T

124115388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529296-C-T

124115771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58529489-C-G

124116512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58530304-C-T

http://identifiers.org/hco/8/GRCh38#124116564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58530341-C-A

124116698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58530471-C-T

124116755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58530524-T-A

124117856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58531261-T-C

124117949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58531345-T-C

124118005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58531422-C-T

124118383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58531781-C-T

124118615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58532027-C-T

http://identifiers.org/hco/8/GRCh38#124118714-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58532499-A-C

124118714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58532499-A-G

124118815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58532576-G-A

124119069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58532788-A-T

124119229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534205-G-A

124119452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534414-C-T

124119466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534430-G-T

http://identifiers.org/hco/8/GRCh38#124119484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534453-C-A

http://identifiers.org/hco/8/GRCh38#124119495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534464-C-A

124119495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534464-C-G

124119495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534464-C-T

124119502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534470-T-C

http://identifiers.org/hco/8/GRCh38#124119594-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534547-C-A

124119594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58534547-C-T

http://identifiers.org/hco/8/GRCh38#124119599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534552-C-A

124119599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58534552-C-G

124119599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 58534552-C-T

124119628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534578-G-A

124119697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534647-T-C

124119792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534735-G-A

124119792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534735-G-C

124119869-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534811-T-A

124119869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534811-T-C

124119936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534920-T-C

http://identifiers.org/hco/8/GRCh38#124119939-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534923-C-A

124119939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534923-C-T

http://identifiers.org/hco/8/GRCh38#124119954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534938-C-A

124119954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534938-C-T

124119975-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534966-T-A

http://identifiers.org/hco/8/GRCh38#124120005-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58534996-A-C

124120005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58534996-A-G

http://identifiers.org/hco/8/GRCh38#124120048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#58535036-C-A

124120048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58535036-C-T

124120146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58535136-T-C

124120579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58535476-T-C

124120797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58535642-C-T

124120908-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58535759-G-C

124120946-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58535797-C-G

124122234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58536987-C-T

124122350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537104-T-C

http://identifiers.org/hco/8/GRCh38#124122388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58537123-C-A

124122388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537123-C-T

124122594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537322-A-G

124122734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537449-T-C

124122996-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537672-A-G

http://identifiers.org/hco/8/GRCh38#124123015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58537690-C-A

124123015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58537690-C-T

124123237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58539165-G-T

124123557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58539437-C-T

124123831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58539698-T-C

124126485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58540562-C-T

124126494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58540571-G-C

http://identifiers.org/hco/8/GRCh38#124126551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58540639-C-A

124126551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58540639-C-T

124126622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58540726-T-G

124126910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541017-A-G

http://identifiers.org/hco/8/GRCh38#124126964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58541068-A-C

124127141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541155-T-G

124127330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541350-A-G

124127346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541367-T-A

http://identifiers.org/hco/8/GRCh38#124127422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58541445-C-A

http://identifiers.org/hco/8/GRCh38#124127653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58541636-C-A

124127765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541779-T-C

124127806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58541867-T-C

124137688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

124137723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

124137741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

124138094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -A-T

124138135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

124138220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -G-A

124138384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: -C-G

124138446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 58543177-T-C

http://identifiers.org/hco/8/GRCh38#124138693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58543509-C-A

124138693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58543509-C-T

http://identifiers.org/hco/8/GRCh38#124146306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58544640-C-A

124146306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544640-C-T

124146390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544707-C-T

124146393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544710-A-G

124146461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544778-T-C

124146461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544778-T-G

124146463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544780-G-A

124146591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544907-A-G

124146609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544925-T-C

124146628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58544943-T-C

124148437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58546892-T-C

124148671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58547127-T-C

124148717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58547173-C-T

124149057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58547510-C-T

124149118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58547576-T-G

124149470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58548634-A-G

124149583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58548742-A-T

124149764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58548922-C-T

http://identifiers.org/hco/8/GRCh38#124149873-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58549049-A-C

124149984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549140-G-A

124149994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549150-G-A

124149994-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549150-G-C

124150093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549237-C-G

124150414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549570-A-G

124150754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549912-C-T

124150792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58549950-T-C

http://identifiers.org/hco/8/GRCh38#124150853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58550022-C-A

124158141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58552257-T-C

http://identifiers.org/hco/8/GRCh38#124158155-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58552267-A-C

124158155-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58552267-A-T

124158346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58552426-T-C

124158346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58552426-T-G

124158356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58552436-G-A

http://identifiers.org/hco/8/GRCh38#124158827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58553011-A-C

124159017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58553203-C-T

124159140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58553604-G-A

124159163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58553626-G-A

124159327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58553779-T-G

http://identifiers.org/hco/8/GRCh38#124159416-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58553818-A-C

124159561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58553957-T-C

124159760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58554171-A-G

124159928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58554459-C-T

124162830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58556164-G-C

124163702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58556559-G-C

http://identifiers.org/hco/8/GRCh38#124163766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58556623-C-A

124164234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557079-T-C

124164268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557113-G-T

http://identifiers.org/hco/8/GRCh38#124164317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#58557168-A-C

124164317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557168-A-G

124164392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557245-T-G

124164532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557354-A-G

124164653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557460-T-C

124169010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557696-G-C

124169207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557862-G-C

124169299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26534
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 58557954-T-C