123392383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33183498-C-G

123392537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33183305-T-C

123392582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33183281-T-C

http://identifiers.org/hco/6/GRCh38#123392625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33183239-A-C

123392818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33183141-A-G

123392958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182987-T-C

123393270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182669-T-C

123393270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182669-T-G

123393273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182657-A-G

123393279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182651-A-G

123393317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182616-G-T

123393419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182511-C-G

123393419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33182511-C-T

123393545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33181167-A-G

123393595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33181115-A-T

http://identifiers.org/hco/6/GRCh38#123393633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33181075-C-A

123393633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33181075-C-T

http://identifiers.org/hco/6/GRCh38#123393642-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33181066-C-A

123393642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33181066-C-T

123393727-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180975-T-A

123393727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180975-T-C

123393732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180970-A-G

123393836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180251-G-A

123393967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180165-T-C

123394002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33180129-T-C

123394315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33179835-A-T

123394444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33179722-A-G

123394483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33179688-G-T

http://identifiers.org/hco/6/GRCh38#123394590-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33179567-A-C

123395709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33177790-C-T

123395989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33177577-A-G

123395994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33177572-C-T

123397159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33177401-G-A

123397277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33177301-A-G

123397689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33176928-T-G

123398795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33175379-G-A

123398853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33175328-T-A

123398950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33175222-C-T

123399094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33175081-C-T

123399155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33175010-G-A

123399183-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33174982-T-A

123399337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33174821-C-G

http://identifiers.org/hco/6/GRCh38#123400758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33164820-C-A

123400893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164691-G-T

123400988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164593-G-A

123401006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164574-C-T

123401136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164440-T-A

123401199-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164372-T-A

123401238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164309-G-A

123401358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164206-G-A

123401411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164152-T-C

123401478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164098-C-T

123401518-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33164068-T-A

123402031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163891-G-A

123402109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163814-C-T

http://identifiers.org/hco/6/GRCh38#123402112-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33163811-A-C

123402135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163784-G-A

123402327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163568-T-A

123402487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163422-T-G

http://identifiers.org/hco/6/GRCh38#123402649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33163159-A-C

123402790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33163021-T-A

123410511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33160494-A-G

http://identifiers.org/hco/6/GRCh38#123410557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33160450-C-A

123410603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33160408-A-T

123410811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33160207-A-T

123410928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33160064-A-G

123413560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33159298-T-C

123413675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33159183-T-C

123413762-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33158859-T-C

123413785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33158835-T-C

123414013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33158635-T-C

123424311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33152051-T-C

123424380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151995-T-C

123424456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151917-C-T

123424481-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151896-T-A

123424497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151881-C-T

123424541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151849-G-T

123424590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151800-G-T

http://identifiers.org/hco/6/GRCh38#123424664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33151726-A-C

123424697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151702-G-A

123424750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151640-G-A

123425133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151168-T-C

123425335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33151041-T-C

123426633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147898-T-A

123426840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147718-T-C

123427227-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147347-T-A

123427227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147347-T-C

123427230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147344-A-T

123427241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33147333-G-A

123434364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138598-G-T

123434375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138587-C-T

123434429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138546-A-G

http://identifiers.org/hco/6/GRCh38#123434519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33138464-A-C

123434519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138464-A-G

123434797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138234-T-G

123434870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138189-C-T

123435075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33138026-G-T

123435104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33137995-A-G

123435166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33137918-T-C

123435285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33137801-T-C

123435530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33137009-C-T

123435841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136700-C-T

123435884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136657-A-G

123435898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136643-A-G

123435939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136604-A-G

123435939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136604-A-T

http://identifiers.org/hco/6/GRCh38#123436518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33136140-C-A

123436518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136140-C-G

123436578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136091-T-A

123436592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136077-G-A

123436632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33136045-T-C

123436953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135726-A-G

123436996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135684-C-T

123437004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135676-C-T

123437065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135617-T-C

123437120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135568-A-G

123437144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33135538-A-T

123437909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33134281-G-C

123438042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33134156-G-A

123438042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33134156-G-T

123438052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33134146-A-G

http://identifiers.org/hco/6/GRCh38#123438139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33134064-A-C

123438271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133930-G-A

123438271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133930-G-T

123438287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133914-C-T

123438547-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133669-T-A

http://identifiers.org/hco/6/GRCh38#123438575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33133632-C-A

123438583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133625-T-G

123438774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33133341-G-A

123439033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132997-A-G

123439078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132956-T-A

http://identifiers.org/hco/6/GRCh38#123439089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33132945-C-A

123439089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132945-C-T

http://identifiers.org/hco/6/GRCh38#123439094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33132940-C-A

123439094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132940-C-T

123439164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132892-A-G

123439194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132858-T-C

123439568-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33132380-T-A

123439774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33132187-T-C

http://identifiers.org/hco/6/GRCh38#123439804-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33132157-A-C

123439919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33132051-G-T

123440102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131868-T-C

123440104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131866-G-C

123440141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131829-T-A

123440141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131829-T-G

123440244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131725-A-G

123440354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131630-C-G

123440483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131503-G-C

123440690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131315-G-A

123440711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131294-T-C

http://identifiers.org/hco/6/GRCh38#123440852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33131159-A-C

123440861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33131150-T-C

123441060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33130943-A-G

123441116-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130888-C-G

123441116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130888-C-T

123441210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130794-T-C

123441577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130468-C-T

123441892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130154-C-T

123441939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130111-A-G

123441971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130079-T-A

123441971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130079-T-C

http://identifiers.org/hco/6/GRCh38#123441974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33130076-C-A

http://identifiers.org/hco/6/GRCh38#123441986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33130064-A-C

123441986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33130064-A-G

123442039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33130011-A-G

123442147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33129912-G-T

123442200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33129869-G-T

http://identifiers.org/hco/6/GRCh38#123442368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33129809-C-A

123442368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129809-C-T

123442625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129754-T-C

123442696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129683-A-T

http://identifiers.org/hco/6/GRCh38#123442703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33129676-C-A

http://identifiers.org/hco/6/GRCh38#123442827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33129562-A-C

123442875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129482-G-A

123442875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129482-G-C

http://identifiers.org/hco/6/GRCh38#123443035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33129197-C-A

123443035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129197-C-G

123443063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129171-T-C

123443124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129103-A-G

123443146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33129088-T-C

123446982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33128101-C-T

http://identifiers.org/hco/6/GRCh38#123454419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33127374-A-C

123455181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33126538-G-A

http://identifiers.org/hco/6/GRCh38#123455199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33126520-C-A

123455277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33126455-T-C

http://identifiers.org/hco/6/GRCh38#123455290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33126442-A-C

123455329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33126403-T-C

123455357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33126375-G-A

123455768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33126039-G-T

123456057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33125771-C-T

123456089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33125727-T-C

123456161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33125650-A-G

123456257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33125550-C-T

123456372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33125439-C-G

123458690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33119655-T-C

123458690-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33119655-T-G

123458758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33119587-C-T

123458946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33119439-G-A

123459113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33119308-C-T

123461240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33118278-A-T

123461266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33118249-T-C

123461280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33118235-G-C

123461372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33118147-T-C

123461518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33118004-T-C

123461527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117995-T-C

123461623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117837-T-C

123461739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117692-G-A

123461979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117473-G-T

123462084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117367-G-A

123462218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117244-T-C

123462221-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117241-A-T

123462223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117239-G-A

123462307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33117163-C-T

123462394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33117078-T-G

123462664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33116789-G-A

123462735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33116730-A-G

http://identifiers.org/hco/6/GRCh38#123462858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33116453-C-A

123462876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33116435-A-G

123462956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33116341-G-T

123463445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33116176-C-G

123463561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33116060-C-G

123463721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33115909-A-G

123464292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110472-C-T

123464339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110426-T-C

123464500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110317-T-C

http://identifiers.org/hco/6/GRCh38#123464605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33110221-C-A

123464692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110142-C-G

123464706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110128-T-C

123464718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110116-A-G

123464718-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110116-A-T

123464748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110089-A-G

123464781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110051-A-G

123464781-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110051-A-T

123464806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110029-T-C

123464806-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33110029-T-G

123464873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33109967-A-G

123464916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33109910-A-G

http://identifiers.org/hco/6/GRCh38#123464987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33109845-C-A

123464987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 33109845-C-T

123465054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33109783-T-A

123465091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33109746-G-T

123465339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33109502-G-A

123465362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33109477-C-T

http://identifiers.org/hco/6/GRCh38#123465966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33108939-A-C

123465980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33108925-C-T

123465988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33108917-G-A

123466055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33108844-T-C

123466163-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33108748-T-G

123467778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33106533-A-G

123467866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33106464-T-C

123468528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105799-T-C

http://identifiers.org/hco/6/GRCh38#123468643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33105695-A-C

123468651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105687-A-T

123468686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105653-T-C

123468693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105650-T-A

123468693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105650-T-C

123468743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105636-T-C

http://identifiers.org/hco/6/GRCh38#123468749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33105630-C-A

123468782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105597-T-C

123468788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33105591-A-T

123468840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33105539-T-C

123469252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33105160-C-T

123469721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104926-G-A

123469721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104926-G-T

123469812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104820-G-T

123469826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104810-G-A

123469826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104810-G-T

123469879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104756-A-G

123469977-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104655-A-T

123470078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104569-G-A

123470097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104546-C-G

http://identifiers.org/hco/6/GRCh38#123470107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33104536-C-A

123470112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104531-A-G

123470112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104531-A-T

123470252-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104348-T-G

123470253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104347-A-T

http://identifiers.org/hco/6/GRCh38#123470532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33104065-C-A

123470568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33104025-G-T

123470639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103949-A-T

123470726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103887-G-T

123470855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103740-A-G

123470938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103663-G-T

123470969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103650-T-C

123471165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103438-T-C

123471168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103435-A-G

http://identifiers.org/hco/6/GRCh38#123471198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33103402-C-A

http://identifiers.org/hco/6/GRCh38#123471210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33103337-A-C

123471224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103269-A-G

123471272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103219-G-T

123471279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103212-T-C

123471285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33103206-C-T

http://identifiers.org/hco/6/GRCh38#123471531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33102910-C-A

123471671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 33102771-C-T

http://identifiers.org/hco/6/GRCh38#123471789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33102653-A-C

123471789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33102653-A-G

http://identifiers.org/hco/6/GRCh38#123472022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33102414-C-A

123472026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33102410-A-G

123478205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33102248-C-T

123478354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33102125-C-T

123478609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101883-A-G

123478667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101797-A-G

123478694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101714-G-A

123478694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101714-G-T

123478996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101350-T-A

123479122-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101222-G-T

123479154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101193-G-T

123479271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33101104-G-A

123479449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33100932-A-T

123480062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33100303-G-A

123480095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33100270-G-A

123480241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33100177-T-A

123480241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33100177-T-C

123480784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093662-G-A

123480794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093652-C-T

123481004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093473-A-T

123481205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093323-A-G

123481296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093232-A-G

123481352-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093172-T-C

123481391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093139-T-A

123481468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093086-A-G

123481472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33093082-T-C

123481640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092921-T-C

http://identifiers.org/hco/6/GRCh38#123481656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33092905-C-A

123481656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092905-C-T

123481661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092900-T-G

123481886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092458-C-T

123482030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092315-T-C

123482094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33092261-T-G

123482434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33091938-G-A

123482603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33091779-A-T

123482910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33091416-G-A

123482944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33091386-G-A

123483487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090984-G-T

123483999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090707-G-C

123484123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090620-C-T

123484156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090589-G-A

123484156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090589-G-C

123484156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090589-G-T

123484266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090541-G-A

123484305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33090501-A-G

http://identifiers.org/hco/6/GRCh38#123484739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33089979-C-A

http://identifiers.org/hco/6/GRCh38#123484799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33089915-A-C

123484799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089915-A-G

123484816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089898-T-C

http://identifiers.org/hco/6/GRCh38#123484934-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33089819-A-C

123485169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089624-C-G

123485286-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089507-A-T

123485392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089403-G-T

123485489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089313-G-T

123485499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089302-G-A

123485767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089063-A-G

123485808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33089021-G-C

123486515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085385-T-C

123486591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085310-T-A

http://identifiers.org/hco/6/GRCh38#123486645-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33085257-A-C

123486809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33085089-A-G

123487102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33084835-G-A

123496558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076828-A-G

123496706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33076696-C-G

123497085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076322-C-T

http://identifiers.org/hco/6/GRCh38#123497134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33076275-C-A

123497134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076275-C-T

123497222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076187-T-A

123497222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076187-T-C

123497228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076181-A-G

123497266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076143-A-G

123497285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076122-A-G

http://identifiers.org/hco/6/GRCh38#123497312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33076095-C-A

123497312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33076095-C-T

123497421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075987-G-C

123497440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075970-G-A

123497837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075621-T-C

123497882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075588-A-G

123498209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075251-T-C

http://identifiers.org/hco/6/GRCh38#123498301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33075177-C-A

123498301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075177-C-T

123498447-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075071-A-T

123498472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075046-C-T

123498498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33075020-T-C

123498557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33074998-G-T

123498638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33074919-T-G

123498644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 33074913-C-G

http://identifiers.org/hco/6/GRCh38#123498661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33074895-A-C

123498661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074895-A-G

http://identifiers.org/hco/6/GRCh38#123498688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33074868-C-A

http://identifiers.org/hco/6/GRCh38#123498700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33074856-C-A

123498700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33074856-C-T

http://identifiers.org/hco/6/GRCh38#123502134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33073662-C-A

123502239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073572-T-C

123502245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073566-A-G

123502247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073564-G-A

123502270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073546-T-A

123502270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073546-T-C

123502312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073507-G-C

123502312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073507-G-T

http://identifiers.org/hco/6/GRCh38#123502456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33073367-A-C

123502456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073367-A-G

123502456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073367-A-T

123502470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073353-A-T

123502561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073227-A-T

123502600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073187-T-C

123502674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33073119-A-G

http://identifiers.org/hco/6/GRCh38#123502757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072997-C-A

123502757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072997-C-G

http://identifiers.org/hco/6/GRCh38#123502815-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072935-A-C

123502840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072910-C-T

http://identifiers.org/hco/6/GRCh38#123502850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072901-C-A

123502850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072901-C-G

123502939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072824-G-A

123502992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072787-T-C

123502992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072787-T-G

123503021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072762-A-G

123503045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072752-T-C

123503117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072691-T-C

123503167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072645-A-G

123503190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072623-C-G

123503315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072496-G-T

123503338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072473-G-A

123503361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072444-C-T

123503379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072429-A-G

http://identifiers.org/hco/6/GRCh38#123503390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072418-A-C

123503402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072417-A-G

123503429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072389-A-G

http://identifiers.org/hco/6/GRCh38#123503507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072315-C-A

123503507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072315-C-T

123503532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072292-T-C

123503536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072288-A-G

123503564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072266-T-C

http://identifiers.org/hco/6/GRCh38#123503609-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33072222-C-A

123503609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072222-C-T

123503822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33072022-C-T

http://identifiers.org/hco/6/GRCh38#123503847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33071997-A-C

123503847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 33071997-A-T

http://identifiers.org/hco/6/GRCh38#123503851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#33071993-C-A

123503940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071914-T-C

http://identifiers.org/hco/6/GRCh38#123503961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33071895-C-A

123503961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071895-C-T

123503978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071882-G-A

123504008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071858-G-T

123504064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071842-A-G

123504148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071746-T-C

123504226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071665-A-G

123504326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071576-G-A

123504401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071505-T-C

123504872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33071041-C-G

123506864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070899-A-T

123507057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070638-T-G

123507124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070571-G-A

123507316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070346-G-A

123507316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070346-G-T

123507430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070237-T-A

http://identifiers.org/hco/6/GRCh38#123508530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33070167-C-A

http://identifiers.org/hco/6/GRCh38#123508545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33070152-C-A

123508546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070151-C-T

123508685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070031-G-A

123508685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33070031-G-T

123508775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069938-T-C

123508852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069897-T-C

123508891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 33069858-G-A

http://identifiers.org/hco/6/GRCh38#123508927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#33069820-A-C

123510461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40592
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 33065415-A-G