http://identifiers.org/hco/3/GRCh38#126394928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90405413-C-A

126394928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405413-C-G

126394937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405402-G-A

126394937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405402-G-T

126394942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405398-G-A

126394942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405398-G-C

126394942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90405398-G-T

126394991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405350-G-A

126395043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405317-G-A

126395043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405317-G-T

126395095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405276-T-C

http://identifiers.org/hco/3/GRCh38#126395178-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90405194-A-C

126395178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405194-A-T

http://identifiers.org/hco/3/GRCh38#126395219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90405144-C-A

126395219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90405144-C-T

http://identifiers.org/hco/3/GRCh38#126395386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90405013-A-C

126395386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 90405013-A-G

126395478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404923-A-T

126395488-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404913-T-G

126395499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404903-T-C

126395499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404903-T-G

126395836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404611-C-T

126395839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404608-A-G

126395899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404567-G-A

126395899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404567-G-T

http://identifiers.org/hco/3/GRCh38#126395902-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404564-C-A

126395902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404564-C-T

126395941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 90404524-G-A

126395941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 90404524-G-T

126395942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90404523-G-A

126395942-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 90404523-G-C

http://identifiers.org/hco/3/GRCh38#126395950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404515-C-A

126396055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404412-T-C

http://identifiers.org/hco/3/GRCh38#126396102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404363-C-A

126396102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404363-C-G

126396102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404363-C-T

http://identifiers.org/hco/3/GRCh38#126396119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404344-C-A

126396119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404344-C-G

126396119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404344-C-T

126396121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404342-G-A

126396129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404334-T-A

126396129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404334-T-C

http://identifiers.org/hco/3/GRCh38#126396200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404304-C-A

126396200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404304-C-T

126396201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404303-C-T

126396404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404115-G-T

126396434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404089-T-C

126396434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404089-T-G

http://identifiers.org/hco/3/GRCh38#126396452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90404071-C-A

126396452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90404071-C-T

126396528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90404011-A-G

126396580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90403958-A-G

http://identifiers.org/hco/3/GRCh38#126396656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90403889-C-A

126396656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90403889-C-T

126396683-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90403854-A-G

126396704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90403835-G-T

126396759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90403785-G-C

126407031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396567-T-C

126407044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396555-G-A

126407044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396555-G-T

http://identifiers.org/hco/3/GRCh38#126407097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90396505-C-A

126407097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396505-C-T

126407111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396491-T-C

126407228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90396380-A-G

http://identifiers.org/hco/3/GRCh38#126407234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90396374-C-A

126407234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90396374-C-G

126407234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90396374-C-T

http://identifiers.org/hco/3/GRCh38#126407281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90396325-C-A

126407281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396325-C-T

126407351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396275-G-A

126407351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396275-G-T

126407394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396234-T-C

126407505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90396155-T-C

126413741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394946-C-T

126413742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394945-A-G

126414222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90394554-T-C

126414222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 90394554-T-G

126414522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394386-G-A

126414522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394386-G-T

126414596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394343-A-G

126414780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394218-T-C

126414894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90394109-T-C

http://identifiers.org/hco/3/GRCh38#126415046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90393942-C-A

126415046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393942-C-G

126415220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393778-G-A

126415428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393644-T-A

126416067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393139-G-A

126416173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393025-T-C

126416173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393025-T-G

126416194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393004-A-G

126416194-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90393004-A-T

126416225-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392962-A-T

http://identifiers.org/hco/3/GRCh38#126416249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90392935-C-A

http://identifiers.org/hco/3/GRCh38#126416307-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90392881-C-A

126416307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392881-C-G

126416307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392881-C-T

126416427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90392761-G-A

126416427-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90392761-G-T

126416459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90392729-T-A

126416505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90392683-A-G

126416514-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392674-T-A

126416514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90392674-T-C

126418400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391071-C-T

126418407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391064-C-T

126418410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391058-C-T

http://identifiers.org/hco/3/GRCh38#126418421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90391047-C-A

http://identifiers.org/hco/3/GRCh38#126418426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90391042-C-A

126418426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391042-C-G

126418426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391042-C-T

126418433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90391036-G-A

126418514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390952-T-C

126418514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390952-T-G

126418659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390807-G-A

126418725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390741-G-A

126418725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390741-G-T

126418769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390697-G-A

126418769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390697-G-T

126418771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90390695-G-T

126418782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90390684-T-A

126418782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 90390684-T-C

126418785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390681-G-A

126418785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390681-G-T

126418992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390508-T-A

126418992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390508-T-C

126418995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390505-G-C

126418995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390505-G-T

126418997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390503-G-A

126419145-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90390370-T-A

126419145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90390370-T-C

126419160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390355-A-G

126419160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390355-A-T

126419383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390185-T-G

126419427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90390144-A-G

126419787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90389856-G-A

126419787-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90389856-G-C

126419809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90389834-G-A

126419830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389813-G-A

126419830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389813-G-C

126419978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 90389373-A-G

126420030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 90389323-C-T

http://identifiers.org/hco/3/GRCh38#126420084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90389278-A-C

126420084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90389278-A-G

http://identifiers.org/hco/3/GRCh38#126423263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90386692-C-A

http://identifiers.org/hco/3/GRCh38#126423267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90386688-C-A

126423267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386688-C-T

126423290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386665-G-A

126423339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90386619-T-C

http://identifiers.org/hco/3/GRCh38#126423740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90386292-C-A

126423740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386292-C-G

126423740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90386292-C-T

126424188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385968-G-A

126424212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385947-G-A

126424212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385947-G-C

http://identifiers.org/hco/3/GRCh38#126424437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90385761-C-A

http://identifiers.org/hco/3/GRCh38#126424761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90385468-A-C

126424868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385382-T-C

126425126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90385140-C-T

126433142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90383998-G-A

126433142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90383998-G-T

126433193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90383947-G-A

126433215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90383931-G-T

126433321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90383893-T-C

126433321-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90383893-T-G

126433359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 90383863-A-G

http://identifiers.org/hco/3/GRCh38#126433626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90383729-C-A

126433626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383729-C-G

126433626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383729-C-T

126433633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90383722-G-T

http://identifiers.org/hco/3/GRCh38#126433641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90383714-A-C

126433641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383714-A-G

126433641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383714-A-T

126433650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383700-T-A

126433650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383700-T-C

126433650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90383700-T-G

126433732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90383641-G-A

126433732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 90383641-G-T

http://identifiers.org/hco/3/GRCh38#126433846-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90383531-A-C

http://identifiers.org/hco/3/GRCh38#126433848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90383529-C-A

126433848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383529-C-T

126433946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383398-A-G

126433946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383398-A-T

126434050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383318-A-G

126434050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383318-A-T

126434088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383286-G-A

126434088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383286-G-T

http://identifiers.org/hco/3/GRCh38#126434105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90383271-C-A

126434105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 90383271-C-T

126435515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90382465-C-T

http://identifiers.org/hco/3/GRCh38#126435554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90382428-C-A

http://identifiers.org/hco/3/GRCh38#126435611-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90382371-C-A

126436087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381161-C-G

126436087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381161-C-T

http://identifiers.org/hco/3/GRCh38#126436166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90381101-C-A

126436166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381101-C-T

126436247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381020-G-A

126436247-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381020-G-T

http://identifiers.org/hco/3/GRCh38#126436253-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90381011-C-A

126436253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90381011-C-T

126436264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 90380999-G-A

126436345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 90380918-C-T

http://identifiers.org/hco/3/GRCh38#126436356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#90380907-C-A

126436374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 90380889-G-A

126436437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26842
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 90380839-C-T