121348990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307108-A-G

121349222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307335-G-A

121349242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307355-C-T

121349311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307435-A-G

http://identifiers.org/hco/7/GRCh38#121349468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22307456-C-A

121349501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307488-T-C

121349631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307606-T-C

121349767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307737-T-C

http://identifiers.org/hco/7/GRCh38#121349829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22307798-C-A

http://identifiers.org/hco/7/GRCh38#121349830-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22307799-A-C

121349857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307822-C-T

121349979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22307962-C-T

121350041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22308024-G-A

121350041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22308024-G-T

121350069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22308057-A-T

121350104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22308092-T-C

121350158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 3 prime UTR variant
orthologous variants: 22308146-A-T

121350568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308555-T-C

121350598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308590-T-C

121350611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308603-T-C

121350664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308657-T-C

121350666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22308659-T-A

121350862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309059-A-G

121350919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309104-T-C

121351020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309196-G-A

121351020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309196-G-T

121351032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309212-A-T

121351042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309222-C-G

121351084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309265-T-C

121351116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309295-T-C

121351134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22309317-G-T

121351230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22309413-C-T

121351318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309493-G-A

121351318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309493-G-T

http://identifiers.org/hco/7/GRCh38#121351331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22309509-C-A

121351331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309509-C-T

121351339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309515-T-C

http://identifiers.org/hco/7/GRCh38#121351351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22309527-A-C

121351351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309527-A-G

121351389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309569-T-A

121351389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309569-T-C

121351390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309570-G-A

121351390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309570-G-T

121351432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309616-T-C

http://identifiers.org/hco/7/GRCh38#121351438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22309622-A-C

121351448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309632-G-A

121351448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309632-G-C

121351448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22309632-G-T

121351581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22309750-T-C

http://identifiers.org/hco/7/GRCh38#121351601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22309771-C-A

121351601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22309771-C-G

121351601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22309771-C-T

121351736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22309858-T-C

121351772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22309889-T-C

http://identifiers.org/hco/7/GRCh38#121351895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22310115-C-A

121351919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310188-A-T

121351982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310254-G-A

121351994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310261-A-G

121351999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310266-T-C

121352077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310332-A-G

121352366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310590-T-C

121352399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310626-T-C

121352407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22310630-G-A

121353162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22311460-T-A

121353425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22311712-T-C

121353495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22311784-C-T

121353517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22311807-G-A

http://identifiers.org/hco/7/GRCh38#121353956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22312595-A-C

121355674-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22315962-T-A

121355805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22316096-G-A

121356184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22316447-C-T

121358547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317317-T-C

121358586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317358-T-C

121358857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317618-T-C

121359002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317763-G-A

121359158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317858-C-T

121359183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317886-T-C

121359354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317956-G-A

121359385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22317983-T-C

121359471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318021-T-C

121359502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318047-T-C

121359581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318127-C-G

121359606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318151-T-C

http://identifiers.org/hco/7/GRCh38#121359670-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22318471-A-C

121359726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318608-A-G

121359919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318813-G-A

121359919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318813-G-T

121359923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318817-G-A

121359923-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318817-G-C

121359923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318817-G-T

121359975-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318859-T-G

121360033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318923-G-A

121360033-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22318923-G-T

121360060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: synonymous variant
orthologous variants: 22318950-G-A

121360060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: stop gained
orthologous variants: 22318950-G-C

121360060-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: stop gained
orthologous variants: 22318950-G-T

121360087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: synonymous variant
orthologous variants: 22318977-A-G

121360139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319029-G-A

121360139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319029-G-T

121360198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319098-G-A

121360198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319098-G-C

121360198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319098-G-T

121360218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319113-T-A

121360218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319113-T-C

121360219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319114-C-T

121360298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319207-G-A

http://identifiers.org/hco/7/GRCh38#121360383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22319320-A-C

121360891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319473-G-A

121361174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319722-G-A

121361287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319833-T-C

121361289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319835-T-C

121361419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319967-C-G

121361419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319967-C-T

121361447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22319994-C-T

121361495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22320041-A-G

121361634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22320176-T-C

121362206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22320585-G-A

121362263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22320637-C-T

121362682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22321175-A-T

121362684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22321177-T-C

121362686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22321179-T-A

121362686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22321179-T-C

121362693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22321186-C-T

121362714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22321199-A-G

121362755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22321231-G-A

http://identifiers.org/hco/7/GRCh38#121362772-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22321248-A-C

121362772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22321248-A-G

121362862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22321293-C-T

121362866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22321297-A-G

121362931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22321362-T-C

http://identifiers.org/hco/7/GRCh38#121363010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22321442-A-C

121363010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321442-A-G

121363131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321518-C-T

http://identifiers.org/hco/7/GRCh38#121363227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22321543-A-C

121363231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321547-T-C

121363321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321636-T-C

121363777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22321928-C-T

121363874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322025-T-C

121363951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322105-C-T

121363952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322106-G-A

121363985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322139-T-C

121364043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322198-C-G

121364061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322214-A-G

121364079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322232-A-G

121364096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322255-G-T

121364097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322256-A-G

121364102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322261-A-G

121364102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322261-A-T

121364119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322278-A-G

121364119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 22322278-A-T

121364149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22322308-G-A

121364149-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 22322308-G-T

121364208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322367-A-G

121364241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322401-T-C

121364260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322417-T-C

121364273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322425-A-G

121364308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322459-G-A

121364308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322459-G-T

http://identifiers.org/hco/7/GRCh38#121364309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22322460-C-A

121364309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322460-C-T

121364313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322464-G-A

121364313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322464-G-T

http://identifiers.org/hco/7/GRCh38#121364330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22322481-C-A

http://identifiers.org/hco/7/GRCh38#121364333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22322484-C-A

121364333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322484-C-T

121364370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322556-A-G

121364378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322564-G-A

121364378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322564-G-T

121364483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322828-G-A

121364483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322828-G-T

121364505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322850-A-G

121364505-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 22322850-A-T

121364563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322922-G-A

121364563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322922-G-T

121364565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322924-G-T

121364582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322940-A-G

http://identifiers.org/hco/7/GRCh38#121364597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22322955-C-A

121364627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322983-G-A

121364627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22322983-G-T

121364684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323038-T-G

121364694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323048-G-A

121364694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323048-G-T

http://identifiers.org/hco/7/GRCh38#121364699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22323053-C-A

121364751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323102-C-T

121364752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323103-G-C

121364846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323196-A-G

121365038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323340-T-C

121365175-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323438-G-C

121365451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323683-A-G

121365566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22323796-A-G

121365673-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324079-A-G

121365700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324106-C-T

121365789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324201-A-G

121365828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324236-G-A

http://identifiers.org/hco/7/GRCh38#121365859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22324267-C-A

121366166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324505-C-T

121366253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324587-T-G

121366291-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324623-T-A

121366292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324624-G-A

121366425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324757-C-T

121366432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324764-A-G

121366493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324815-C-G

121366493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324815-C-T

121366586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324896-G-A

121366596-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22324906-T-G

121366654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22325443-T-C

121366918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22325699-T-A

121367115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22325887-A-G

121369316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22326968-G-A

http://identifiers.org/hco/7/GRCh38#121369368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22327020-C-A

121369563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22327331-G-A

121369611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22327379-C-G

121369979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22327497-T-A

121369991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22327509-G-A

121370230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22327705-C-T

121370639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328046-T-C

121370661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328067-T-C

121370661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328067-T-G

121370747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328147-G-C

121370810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328188-G-A

121370844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328221-C-T

121370861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328238-C-T

121371275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328529-T-A

121371275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328529-T-C

121371377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: synonymous variant
orthologous variants: 22328631-A-G

121371407-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: missense variant
orthologous variants: 22328661-T-A

121371407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: synonymous variant
orthologous variants: 22328661-T-C

121371445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328699-G-A

121371506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328766-A-T

121371511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328771-G-A

121371511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328771-G-C

121371511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328771-G-T

121371526-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328787-T-A

121371526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328787-T-C

121371574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328908-T-A

121371574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22328908-T-C

http://identifiers.org/hco/7/GRCh38#121371591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22329004-A-C

http://identifiers.org/hco/7/GRCh38#121371593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22329006-A-C

121371593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329006-A-T

121371876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329368-C-T

121371908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329406-G-A

121371968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329464-A-G

http://identifiers.org/hco/7/GRCh38#121372131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22329599-C-A

121372131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: missense variant
orthologous variants: 22329599-C-T

121372132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: synonymous variant
orthologous variants: 22329600-T-C

http://identifiers.org/hco/7/GRCh38#121372178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22329648-C-A

121372178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329648-C-T

121372206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329674-T-C

121372234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329697-A-G

121372237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329700-A-G

http://identifiers.org/hco/7/GRCh38#121372257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22329720-A-C

121372257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329720-A-G

121372316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329783-A-G

121372353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329826-T-G

121372479-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22329936-T-A

121372548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22330020-T-C

http://identifiers.org/hco/7/GRCh38#121372563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22330035-C-A

121372563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22330035-C-T

121372635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22330161-A-G

121372790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22330312-G-A

121373252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332364-G-A

http://identifiers.org/hco/7/GRCh38#121373391-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22332497-A-C

121373416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332522-C-T

121373464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332575-C-T

121373513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332622-T-C

121373585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332688-A-G

121373670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332774-A-G

121373716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22332820-A-G

http://identifiers.org/hco/7/GRCh38#121373720-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22332824-A-C

121374351-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22333283-C-G

121378639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22334897-G-A

121378639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22334897-G-C

121378801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22335083-T-C

121378801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22335083-T-G

121378856-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22335115-A-T

121378892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339254-G-A

121378892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339254-G-C

121378892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339254-G-T

121379010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 22339372-A-G

121379079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339439-T-C

121379203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339565-C-T

121379356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339730-T-C

121379668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22339996-C-T

121379759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22340476-C-T

121380147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22340985-T-C

121380279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22341157-T-C

121381223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22341708-T-C

121381223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22341708-T-G

121381690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342005-A-G

121381692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342007-G-A

121381692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342007-G-C

121381692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342007-G-T

121382146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342431-G-A

121382187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342471-T-A

121382187-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342471-T-G

121382603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342839-G-A

121382603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342839-G-T

http://identifiers.org/hco/7/GRCh38#121382811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22342942-C-A

121382811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22342942-C-T

http://identifiers.org/hco/7/GRCh38#121382815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22342946-C-A

121382938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343242-A-G

121382971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343279-T-C

121382990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343298-G-A

121382990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343298-G-C

121382990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343298-G-T

121383000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343308-T-A

121383000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22343308-T-C

121383124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343436-T-A

121383138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343453-G-A

121383138-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343453-G-C

121383138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343453-G-T

121383192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343541-G-A

121383257-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343595-C-G

121383287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343621-T-C

121383302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343636-T-C

121383374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343700-T-C

121383452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22343769-T-A

121383716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22344218-T-C

121383729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22344231-G-A

121384202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22344671-T-C

121384283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22344754-A-G

http://identifiers.org/hco/7/GRCh38#121384549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22345033-C-A

121384581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345063-T-G

121384648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345123-A-G

121384837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345460-A-G

121384860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345486-G-A

121384867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345493-T-G

121384873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345500-T-C

121384888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345515-C-T

121384916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345535-T-C

121384924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22345543-C-T

121385385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22346098-T-C

121385414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22346127-C-T

121385447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22346165-A-G

http://identifiers.org/hco/7/GRCh38#121385523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#22346240-A-C

121385523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 22346240-A-G

121385918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 22346522-G-A

121385993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 22346571-A-G

121386108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 22346681-C-G

121386260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22346833-G-A

121386300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22346869-C-T

121386469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348342-T-C

121386548-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348416-T-A

121386548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348416-T-G

121386704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348536-T-C

121386905-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348725-A-T

121387019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22348962-T-G

121387099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349172-A-G

121387106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349179-C-T

121387114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349187-T-C

121387502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349538-T-C

121387567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349600-G-A

121387567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349600-G-C

121387826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349835-T-C

121387894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349894-C-G

121387970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22349960-G-A

121388199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22350634-T-G

121388423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22350964-T-C

121388663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22351226-G-A

121388761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22351411-G-T

121388857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22351473-C-T

121388934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22351547-T-C

http://identifiers.org/hco/7/GRCh38#121389116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22351694-C-A

http://identifiers.org/hco/7/GRCh38#121389232-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22351797-A-C

121389537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 22352084-C-T

121389543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352090-T-C

121389688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352221-T-A

121389701-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352232-T-C

http://identifiers.org/hco/7/GRCh38#121389720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22352251-C-A

http://identifiers.org/hco/7/GRCh38#121389751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22352278-C-A

121389751-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352278-C-G

121389751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352278-C-T

121389893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22352380-T-C

121390734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22353130-T-C

121390816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22353198-C-T

http://identifiers.org/hco/7/GRCh38#121390883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22353259-A-C

121390883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22353259-A-G

121391048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22353436-G-A

121391497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22354015-G-A

121391629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22354128-G-A

121391703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22354202-G-C

121392607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: intron variant
orthologous variants: 22354322-T-G

121395456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22355420-T-C

121395704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22355647-C-T

121395812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22355752-G-A

http://identifiers.org/hco/7/GRCh38#121396161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22355971-C-A

121396161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant, splice_donor_variant
orthologous variants: 22355971-C-T

121396171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22355981-G-A

121396171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22355981-G-T

http://identifiers.org/hco/7/GRCh38#121396210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22356009-C-A

121396210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22356009-C-T

http://identifiers.org/hco/7/GRCh38#121396255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#22356075-C-A

121396255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 22356075-C-T

121396360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 18664
most severe consequence: 5 prime UTR variant
orthologous variants: 22356176-G-A