http://identifiers.org/hco/5/GRCh38#138946725-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399241-A-C

138946725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: 35399241-A-G

138946725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: 35399241-A-T

138946733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: 35399249-T-C

138946733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: 35399249-T-G

http://identifiers.org/hco/5/GRCh38#138946829-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399315-A-C

http://identifiers.org/hco/5/GRCh38#138946912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399377-C-A

http://identifiers.org/hco/5/GRCh38#138946920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399385-C-A

138946920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3 prime UTR variant
orthologous variants: 35399385-C-G

http://identifiers.org/hco/5/GRCh38#138947023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399483-C-A

138947023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35399483-C-T

138947034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35399494-T-C

http://identifiers.org/hco/5/GRCh38#138947038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35399522-C-A

138947096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 35399578-G-C

138947177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35399666-G-A

138947444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35399933-G-A

138947552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35400017-G-A

138947552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35400017-G-T

138947560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35400025-T-G

http://identifiers.org/hco/5/GRCh38#138947590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35400078-C-A

138947673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35400174-T-C

138950284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35401399-C-T

138950424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401504-A-G

138950431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401511-G-A

138950431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401511-G-T

138950450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401523-G-A

138950450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401523-G-C

138950450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401523-G-T

138950508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401573-C-G

138950550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401594-C-T

138950582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401610-C-G

138950582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401610-C-T

138950588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401616-G-A

138950589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401617-C-T

138950602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401625-A-G

138950611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401634-G-A

http://identifiers.org/hco/5/GRCh38#138951021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35401959-A-C

138951021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401959-A-G

http://identifiers.org/hco/5/GRCh38#138951024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35401962-C-A

http://identifiers.org/hco/5/GRCh38#138951029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35401967-C-A

138951029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35401967-C-T

138951080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402008-G-A

138951080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402008-G-T

138951107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402021-G-A

138951107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402021-G-C

http://identifiers.org/hco/5/GRCh38#138951234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35402155-C-A

138951342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 35402263-G-A

http://identifiers.org/hco/5/GRCh38#138951373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35402304-C-A

138951373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402304-C-T

138951593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402511-G-A

138951649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402559-G-A

138951649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402559-G-T

http://identifiers.org/hco/5/GRCh38#138951686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35402591-C-A

138951686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402591-C-T

138951706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402603-C-T

138951746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402629-G-A

138951746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402629-G-T

138951760-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402636-G-T

138951773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35402649-G-T

138951872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 35402751-G-T

138951904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35402784-C-G

http://identifiers.org/hco/5/GRCh38#138951920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35402799-C-A

138951920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35402799-C-T

138952010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35402835-A-G

138952011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35402836-A-G

http://identifiers.org/hco/5/GRCh38#138952029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35402854-A-C

138952142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35402964-G-A

138952263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35403083-T-C

138952698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35403438-G-T

http://identifiers.org/hco/5/GRCh38#138953193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35403816-C-A

138953193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35403816-C-T

138953215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35403836-G-A

http://identifiers.org/hco/5/GRCh38#138953228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35403848-C-A

http://identifiers.org/hco/5/GRCh38#138953443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35404082-C-A

138953443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35404082-C-G

138953443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35404082-C-T

138953452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35404086-T-C

http://identifiers.org/hco/5/GRCh38#138953809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35404408-C-A

138953883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35404484-C-T

http://identifiers.org/hco/5/GRCh38#138954138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35404677-C-A

138954152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35404691-C-G

138954152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35404691-C-T

138954354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35404846-G-A

138954362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35404855-T-A

138954728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35405195-G-A

http://identifiers.org/hco/5/GRCh38#138955035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35405448-A-C

138955176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35405550-C-T

138955177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35405551-G-A

138955299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35405677-A-G

138955572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35405935-G-A

138955645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406008-C-T

138955705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406067-C-T

138955756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406111-T-C

138955926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406274-T-A

138955926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406274-T-C

138956021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406372-G-A

138956045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406396-C-G

138956045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406396-C-T

138956278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406592-A-G

138956481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406803-C-T

http://identifiers.org/hco/5/GRCh38#138956518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35406838-C-A

138956518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35406838-C-T

138960758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35410792-A-T

138960862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35410882-G-A

138960909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35410928-T-C

138960967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35410985-G-A

138962623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412476-T-G

138962680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412513-G-C

138962684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412517-G-A

138962698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412531-G-T

138963129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412971-T-A

138963129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35412971-T-C

138963168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413010-G-C

138963173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413015-T-C

138963354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413199-A-G

138963724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413537-A-G

138963807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413619-T-C

138963924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35413801-A-G

138964114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35414224-A-T

138965459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35415665-C-T

138965537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35415741-A-T

138965666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35415857-T-C

138965760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35415914-C-T

138966066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416009-G-A

138966066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416009-G-T

http://identifiers.org/hco/5/GRCh38#138966256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35416184-A-C

138966276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416204-C-T

138966541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416494-C-T

138966744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416685-T-G

138966832-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416744-A-T

138967056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416925-T-G

138967075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416944-A-G

138967100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35416967-C-T

138967530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417375-T-C

138967654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417495-T-C

http://identifiers.org/hco/5/GRCh38#138967774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35417649-C-A

138967774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417649-C-G

138967938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417816-G-A

138967988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417864-G-A

138968042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35417919-A-G

http://identifiers.org/hco/5/GRCh38#138968187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35418022-C-A

138968187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418022-C-T

138968192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418027-G-A

138968192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418027-G-C

138968192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418027-G-T

138968226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418057-C-T

138968445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418158-G-C

http://identifiers.org/hco/5/GRCh38#138968795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35418460-C-A

http://identifiers.org/hco/5/GRCh38#138968850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35418530-C-A

138968893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418571-G-A

138968912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418591-G-A

138969288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35418919-C-G

138969393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35419003-T-C

138969856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35419434-C-T

138971707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35420435-G-A

138972269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421002-C-T

138972406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421138-T-C

138972429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421159-A-G

138972453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421183-C-T

138972459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421189-T-C

138972980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35421695-C-T

138973455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422023-A-G

138973523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422059-G-A

138974016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422259-C-T

138974668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422748-A-G

138974669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422749-G-A

138974728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422805-C-T

138974845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35422890-C-T

138975809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35423235-G-A

138975960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423351-T-C

138976061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35423437-G-A

138979636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35425013-T-G

138979653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35425030-G-A

138979790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35425159-T-C

138979790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35425159-T-G

138981296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35426257-C-T

138981770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35426694-T-C

138981981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35426832-C-T

138982315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427148-G-A

138982725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427504-G-C

138982725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427504-G-T

138982840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427608-C-T

138982841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427609-G-A

138983638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427769-G-A

138983673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35427805-G-A

138983893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428035-A-G

138984195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428307-A-G

138984349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428413-C-G

138984349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428413-C-T

138984386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428449-G-T

138984647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428585-C-T

138984776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428700-A-G

138984886-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35428790-G-C

138985132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35429304-A-T

138985505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35429665-G-A

138985537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35429695-G-C

138985920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35429995-C-T

http://identifiers.org/hco/5/GRCh38#138986186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35430329-C-A

138986293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35430433-C-G

138986592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35430709-C-T

http://identifiers.org/hco/5/GRCh38#138986707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35430825-C-A

138986860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35430977-C-G

138987689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35431458-C-G

138988256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35431728-A-G

138988361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35431824-C-T

138988642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35432095-C-T

138988895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35432219-T-A

138989644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35432718-A-G

138990424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35433429-C-G

138991178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35433632-G-T

138991372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35433797-A-G

138991408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35433833-G-C

138991805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35434184-C-T

138992174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435310-G-A

138992200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435336-C-T

138992201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435337-T-C

138992316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435443-T-C

138992480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435560-C-T

138992522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435588-A-G

138992538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35435603-T-A

138993642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35438284-T-C

138993817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35438432-G-C

139013651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35444073-C-G

139014101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35444483-A-G

139014854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35444875-A-G

139015538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35445737-A-G

139015585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35445755-C-T

139015706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35445877-A-G

139017171-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35448095-G-T

139017251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35448135-G-A

139017251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35448135-G-T

139017709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35448528-C-T

139017901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35448713-G-A

139018042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35448840-G-A

139018700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449149-G-T

139018715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449166-A-G

139019702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449890-T-G

http://identifiers.org/hco/5/GRCh38#139019756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35449939-C-A

139019756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449939-C-T

139019766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449949-C-T

139019770-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449953-T-A

139019770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35449953-T-C

http://identifiers.org/hco/5/GRCh38#139019927-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35450094-A-C

139020087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35450199-G-C

139020470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35450505-T-C

139020549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35450568-A-G

139020770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35450758-C-T

139021185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35450909-G-A

139021185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 35450909-G-T

139021317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451041-C-G

139021317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451041-C-T

139021386-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451109-T-A

139021418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451140-T-C

139021521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451250-C-T

139021714-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451437-G-T

139021736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451459-G-A

139021736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35451459-G-T

139021847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35453514-G-T

http://identifiers.org/hco/5/GRCh38#139022072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35453724-C-A

139022276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35453913-G-T

139022300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35453937-T-C

http://identifiers.org/hco/5/GRCh38#139022431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35454069-C-A

139022547-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35454172-T-C

139022966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35454371-G-A

139023638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35454961-G-A

139023681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35455003-G-A

139023997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35455315-T-C

139024063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35455374-G-A

139024516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35455788-T-A

http://identifiers.org/hco/5/GRCh38#139025614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35456796-C-A

139025614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35456796-C-T

http://identifiers.org/hco/5/GRCh38#139027105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35458636-C-A

139027133-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35458654-T-A

139027133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35458654-T-C

139027387-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35458888-C-G

139027404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35458903-T-G

139027671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35459155-G-A

139027963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35459442-G-A

139028138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35459602-T-C

139028445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35459709-C-T

139028481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35459738-G-C

139028779-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35460031-A-T

139039959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35471373-T-C

139039987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35471401-T-C

139041681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35472820-G-A

http://identifiers.org/hco/5/GRCh38#139041839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35473054-A-C

139041863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473077-G-A

http://identifiers.org/hco/5/GRCh38#139041877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35473090-A-C

139042035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473267-G-A

139042274-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473786-A-T

139042359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473923-A-G

139042373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473937-G-A

139042434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35473991-G-A

139042476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474032-T-C

139042563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474116-G-A

139042563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474116-G-T

http://identifiers.org/hco/5/GRCh38#139042601-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35474132-A-C

139042601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474132-A-G

139043110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474383-G-C

139043563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35474752-G-C

139044305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35476745-G-A

139044338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35476778-A-G

139044355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35476795-G-A

139044355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35476795-G-C

http://identifiers.org/hco/5/GRCh38#139044386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35476828-C-A

139047138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35479690-A-G

139047552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35480000-T-C

139047574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35480022-T-G

139047664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35480105-T-G

139048770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35480524-G-A

139049055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35480805-A-G

http://identifiers.org/hco/5/GRCh38#139050452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35481021-A-C

139050489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35481058-T-A

139050635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35481204-T-C

139051124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35481900-G-A

139051124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35481900-G-C

139051124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35481900-G-T

http://identifiers.org/hco/5/GRCh38#139051181-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35481983-C-A

139051181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35481983-C-G

139051290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482075-A-G

139051290-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482075-A-T

139051354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482152-T-C

139051479-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482271-G-C

139051544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482326-C-T

139051649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482418-C-T

139051682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35482651-G-T

139054341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35485702-T-C

139054643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35485917-G-A

139054835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486104-G-A

139055031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486277-A-T

139055141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486369-T-C

139055166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486394-T-A

139055529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486671-T-A

139055529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486671-T-C

139055542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35486684-G-A

139060156-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35489025-T-G

139060851-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35489830-G-C

139061155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35490362-G-T

139061276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35490474-C-G

139061276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35490474-C-T

http://identifiers.org/hco/5/GRCh38#139061442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35490630-C-A

139062237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35492264-G-C

139062566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35492593-C-G

139063051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35493179-G-A

139063380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35493481-C-T

139063501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35493850-T-C

http://identifiers.org/hco/5/GRCh38#139063946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35494289-C-A

139064435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35494751-T-G

139064618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35494971-C-T

http://identifiers.org/hco/5/GRCh38#139064638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35494989-C-A

139064651-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495002-T-G

139064921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495257-G-A

139065053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495370-G-A

139065604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495854-A-G

139065645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495895-T-G

139065764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35495993-G-C

139065784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35496013-C-T

139066102-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35496240-A-T

139067679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35496511-T-C

139067716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35496522-G-A

http://identifiers.org/hco/5/GRCh38#139067786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35496582-C-A

139075590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35501939-G-A

139075830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35502163-C-G

139075926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35502254-G-A

http://identifiers.org/hco/5/GRCh38#139076414-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35502722-A-C

139076502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35502808-T-C

139076833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503137-G-A

http://identifiers.org/hco/5/GRCh38#139077214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35503190-C-A

139077214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503190-C-G

139077214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503190-C-T

139077386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503339-A-G

139077538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503480-G-A

139077665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503593-T-C

http://identifiers.org/hco/5/GRCh38#139077712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35503640-A-C

http://identifiers.org/hco/5/GRCh38#139077774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35503696-A-C

139077914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35503808-T-C

139078397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35504127-T-A

139078688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35504380-C-T

139078689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35504381-G-A

139078829-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35504964-G-T

139079777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35505879-T-C

139080106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35506441-G-A

139080134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35506526-A-G

139080595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35508195-G-A

http://identifiers.org/hco/5/GRCh38#139081883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35510478-A-C

http://identifiers.org/hco/5/GRCh38#139081908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35510508-C-A

http://identifiers.org/hco/5/GRCh38#139082036-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35510633-A-C

http://identifiers.org/hco/5/GRCh38#139082059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35510656-C-A

139082079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35510689-C-T

139082082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35510725-C-T

139082150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35510796-G-T

139082526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35511161-G-A

139082577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35511212-T-G

http://identifiers.org/hco/5/GRCh38#139082669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35513749-C-A

139082898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35513974-G-A

139082934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35514019-A-G

139085012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35514660-G-A

139085510-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35515403-T-G

139085943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35515826-T-C

http://identifiers.org/hco/5/GRCh38#139086083-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35515939-A-C

http://identifiers.org/hco/5/GRCh38#139086100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35515956-A-C

139086100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35515956-A-T

139087174-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516081-C-G

139087235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516145-G-A

139087365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516276-T-C

139087622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516419-G-A

139087756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516529-G-A

139087849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35516597-G-A

139088698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35517376-T-C

http://identifiers.org/hco/5/GRCh38#139089652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35518132-A-C

139089652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35518132-A-G

139090360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35518727-T-C

http://identifiers.org/hco/5/GRCh38#139090482-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35518881-A-C

139090617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35519016-G-A

139090858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35519748-A-G

139090874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35519758-G-A

139090940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35519828-T-C

http://identifiers.org/hco/5/GRCh38#139091754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35521033-A-C

139092567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35521804-T-C

http://identifiers.org/hco/5/GRCh38#139092662-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35521900-A-C

139092662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35521900-A-G

139092662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35521900-A-T

139100216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35529727-A-G

http://identifiers.org/hco/5/GRCh38#139100896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35530376-A-C

139101154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35530609-T-C

139101570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35531034-C-G

139101640-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35531096-T-A

139101669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35531122-C-T

139101707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35531159-T-C

139101749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35531184-G-A

139102318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35532934-G-A

139102318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35532934-G-C

139102386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533000-G-A

139102751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533257-G-A

139102751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533257-G-T

139102800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533277-C-T

139102873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533296-C-T

139103174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533462-C-T

139103193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533481-G-A

139103198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533485-A-T

139103381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35533655-A-T

http://identifiers.org/hco/5/GRCh38#139103405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35533679-C-A

139103730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35534005-C-G

139104634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35534416-A-G

139104988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35534695-C-T

139105134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35534825-T-C

139105542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535240-G-A

139105586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535284-T-C

139105630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535328-T-C

139105662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535360-G-T

139105691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535389-G-A

139105691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535389-G-T

139106151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535835-G-A

139106151-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35535835-G-C

139106875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536567-C-G

139106875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536567-C-T

139107096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536790-C-G

139107096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536790-C-T

139107113-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536806-T-G

139107295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35536965-T-C

139107642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35537291-C-G

139107642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron variant
orthologous variants: 35537291-C-T

139108027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35538383-G-A

139108027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35538383-G-T

139108146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 35538483-A-G

139108262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35538590-G-C

139108267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35538595-G-A

139108450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35538978-C-T

139108556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35539081-A-G

139108624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35539148-G-C

139108919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540025-G-A

139108919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540025-G-C

139109415-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540237-A-T

139109489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540308-G-A

139110413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540814-C-T

139110596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35540994-T-C

139110816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35541215-G-A

139113636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35541526-C-T

139114156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35542039-T-C

http://identifiers.org/hco/5/GRCh38#139114477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35542346-C-A

139114592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35545915-T-C

139115407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35546805-T-C

http://identifiers.org/hco/5/GRCh38#139116056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35547393-C-A

139116088-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35547420-C-G

139116440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35547759-T-C

139116543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35547856-C-T

139117958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549039-C-T

139118168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549271-C-G

139118168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549271-C-T

139118415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549506-G-A

139118438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549528-C-T

139119280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549750-G-T

139119314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549782-G-A

139119372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549834-G-A

139119443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549901-C-T

139119812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35549960-T-C

139120182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35550305-T-C

139120429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35550549-C-T

139120446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35550566-C-T

139120829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35550938-A-G

139121012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551088-G-A

139121021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551097-G-A

139121021-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551097-G-C

http://identifiers.org/hco/5/GRCh38#139121233-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35551301-A-C

139121233-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551301-A-G

139121258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551324-T-C

139121281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551344-A-G

139121281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551344-A-T

139121310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551373-T-C

139121407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551466-T-C

139121474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551531-G-A

139121858-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551776-G-C

139121974-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551874-T-G

139122071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35551931-T-C

139123255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35553300-G-A

139123419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35553497-A-G

139123586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35553851-G-A

139124264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35557802-T-C

139124338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35566516-G-T

139124930-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35566986-T-G

139124933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35566989-A-G

139125168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35567204-G-A

139125769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35568330-T-C

139126093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35569170-G-T

139126675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35570017-C-T

139127628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571215-T-A

139127628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571215-T-G

139127631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571218-G-A

139127631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571218-G-T

139127686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571270-G-A

139127686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571270-G-T

139127863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571443-C-T

139127876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571456-C-G

139127878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571458-G-T

139127905-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571478-T-A

139127905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571478-T-C

http://identifiers.org/hco/5/GRCh38#139128007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35571585-C-A

139128007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35571585-C-G

139128039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35571600-A-G

139128043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35571604-G-C

139128043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35571604-G-T

139128161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571697-T-A

139128161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571697-T-C

139128193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571731-T-C

139128301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571835-G-A

139128373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35571907-T-C

139128707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572188-G-A

139128707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572188-G-T

139128826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572280-G-A

http://identifiers.org/hco/5/GRCh38#139128886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35572352-C-A

139129002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572444-C-T

139129014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572456-G-A

139129040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572481-A-G

139129041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572482-G-T

http://identifiers.org/hco/5/GRCh38#139130851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35572739-A-C

139130910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35572797-T-G

139131180-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35573043-T-A

139131755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35573600-T-C

139131826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35573663-G-C

139131826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35573663-G-T

139131903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35573731-A-G

139132298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574217-T-G

139132363-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574279-T-A

139132680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574541-T-C

139133014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574829-C-T

139133201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574992-G-A

139133201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574992-G-C

139133201-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35574992-G-T

139133355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35575142-T-A

http://identifiers.org/hco/5/GRCh38#139133382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35575168-C-A

139133382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35575168-C-T

139133445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35575238-G-A

139133445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35575238-G-C

139133445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35575238-G-T

http://identifiers.org/hco/5/GRCh38#139133509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35575303-C-A

139133509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575303-C-T

139133530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575324-T-C

139133563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575359-G-A

139133605-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575401-C-G

139133647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575449-C-T

139133759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35575576-A-T

139134418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35576172-G-A

139135183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35576848-C-T

139135301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35576951-G-T

139136345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35577573-G-A

139136422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35577647-C-G

139136675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35579830-G-A

139137360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580432-G-A

139137392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580465-G-T

139137454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 35580528-G-A

139137495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35580569-A-G

http://identifiers.org/hco/5/GRCh38#139138412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35580811-A-C

139138459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35580858-G-T

139138516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35580917-C-G

139138518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35580919-C-T

139139077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35581464-G-T

139140329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35582679-G-A

139140640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35583001-G-A

139141281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35584652-A-G

139141498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35584889-A-T

139141968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585243-T-A

139141968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585243-T-C

139142130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35585390-G-T

139147396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588077-C-T

139147397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588078-A-G

139147419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588098-T-C

139147540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588212-T-A

139147562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588234-T-G

139147842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588622-A-G

139147981-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588755-A-T

139148112-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35588894-T-A

139148323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589079-G-C

139148472-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589222-C-G

139148472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589222-C-T

139148511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589261-G-A

139148540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589287-T-G

139148977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589936-C-T

139149020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35589979-C-G

139149533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35590506-C-T

139149761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591001-G-T

139149818-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591059-T-C

139150136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591314-T-C

139150148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591326-T-C

139150263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591439-T-C

http://identifiers.org/hco/5/GRCh38#139150274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35591450-A-C

139150375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591557-C-T

139150473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591635-C-G

http://identifiers.org/hco/5/GRCh38#139150680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35591828-C-A

139150765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591907-G-A

139150785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591926-G-A

139150785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35591926-G-T

139150906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35592048-C-T

139150914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35592058-T-C

139151432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35592551-G-A

139151564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35592681-A-G

139152137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593226-C-T

139152141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593230-C-T

139152169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35593258-G-T

139153535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35594544-G-T

http://identifiers.org/hco/5/GRCh38#139153597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35594676-C-A

139153597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35594676-C-T

139154136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595367-G-A

139154136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35595367-G-T

139154424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35596243-T-C

139154467-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35596287-A-G

139154524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35596340-G-A

http://identifiers.org/hco/5/GRCh38#139154758-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35596570-A-C

139154897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35596702-A-G

139155232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35597041-C-T

139155239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35597048-A-G

139156607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35601042-C-G

139157596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35601926-C-T

139158749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603079-A-G

http://identifiers.org/hco/5/GRCh38#139159069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35603396-A-C

139159133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603493-T-C

139159144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35603503-T-C

139159560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604071-G-A

139159562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604073-G-A

139159638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604145-C-T

139159698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604204-T-C

139159750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604248-T-C

139159835-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604342-T-A

http://identifiers.org/hco/5/GRCh38#139159849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35604356-A-C

139159849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604356-A-G

139159873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604381-C-T

139159934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604497-C-T

http://identifiers.org/hco/5/GRCh38#139160005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35604680-C-A

139160272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604889-G-A

139160272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604889-G-C

139160272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604889-G-T

139160289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604906-T-G

139160363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35604980-A-G

139160470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605065-A-G

139161390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605732-T-A

http://identifiers.org/hco/5/GRCh38#139161530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35605837-A-C

139161544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35605851-G-A

139162081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606048-T-A

139162081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35606048-T-C

139177620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35608638-A-G

139178650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35612177-C-T

139179650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35613164-G-C

139181211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35615123-C-T

139182631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616502-G-A

139183126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35616959-G-A

139183184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35617019-G-A

139183402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35617674-C-T

139183486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35617756-T-C

139183693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35617957-G-A

139183756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35618018-G-A

139184710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35618736-T-C

139185909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620287-C-T

139185936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35620314-G-A

139186872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35621797-G-A

139186961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35621875-G-C

139188462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35622949-G-C

139188474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35622961-G-A

139189983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623336-G-A

139190380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35623716-G-A

139190447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35624165-G-A

139191985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625393-G-T

139192222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625608-T-A

139192222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625608-T-C

139192319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35625683-A-G

http://identifiers.org/hco/5/GRCh38#139192459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35625822-C-A

http://identifiers.org/hco/5/GRCh38#139196429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35629838-C-A

139197086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35630534-T-C

http://identifiers.org/hco/5/GRCh38#139198185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35631744-C-A

139198185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35631744-C-T

139198200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35631759-G-T

http://identifiers.org/hco/5/GRCh38#139198219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35631795-C-A

139198369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35631949-G-A

139198417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35631997-G-A

http://identifiers.org/hco/5/GRCh38#139198422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35632002-C-A

http://identifiers.org/hco/5/GRCh38#139198443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35632023-C-A

139198443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632023-C-T

139198457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35632037-C-T

139198514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35632115-C-T

http://identifiers.org/hco/5/GRCh38#139199581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35633144-A-C

139199740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35633309-G-A

139199746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35633315-C-G

139203666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35635377-T-C

139203861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35635573-G-A

139204275-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35635955-C-G

139204275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35635955-C-T

139207395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638165-G-A

139207673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638447-G-A

139208152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35638898-A-G

139208353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35639068-C-G

139209181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35639890-C-T

139209250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35639958-G-A

139209526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35640220-C-T

139214063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35644410-C-T

139214115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35644462-A-G

139214321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35644656-A-T

139214389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35644937-T-C

http://identifiers.org/hco/5/GRCh38#139214539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35645091-C-A

139214873-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35645455-T-A

139215132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35645702-C-T

139215246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35645820-G-A

139215398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35645975-C-T

139215710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35646977-G-A

139215710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35646977-G-C

http://identifiers.org/hco/5/GRCh38#139221858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35650139-C-A

139221858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35650139-C-T

139222319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35650575-G-T

139222322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35650578-T-A

http://identifiers.org/hco/5/GRCh38#139222729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35650972-A-C

139222729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35650972-A-G

139223367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651397-A-G

139223549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35651554-C-G

139240887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35655390-C-G

139240887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35655390-C-T

139241083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35655574-G-C

139241738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35656813-G-A

139242091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35657165-A-G

139246075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35662659-T-C

139246440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35662992-G-A

139247407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35663624-C-G

139258063-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666365-A-T

139258225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666478-T-C

139258269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35666517-T-C

http://identifiers.org/hco/5/GRCh38#139258663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35668076-A-C

139258747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35668180-T-C

139258767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35668200-A-T

139258995-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35668484-A-T

139259760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669163-T-C

139259941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35669254-G-A

139261876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672360-G-A

139261876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672360-G-T

139262000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672460-G-C

139262265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672782-C-T

http://identifiers.org/hco/5/GRCh38#139262340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35672856-C-A

139262340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672856-C-G

139262460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35672971-C-T

139262535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673034-T-C

139262668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35673125-C-T

139262815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35673253-G-T

139262854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35673292-G-A

139262964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673406-C-T

139263334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35673781-A-G

139263624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674342-A-G

139263748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35674466-T-C

139263778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674501-C-T

139263931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674704-A-G

139264164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35674947-A-G

139264752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676419-G-A

139264767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676423-T-A

139264799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35676454-C-T

139267710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35681025-T-C

139268111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35681557-A-G

139268227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35681664-A-G

139268957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682510-A-G

139268962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35682515-T-C

139271517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35683600-A-G

139271517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35683600-A-T

139271561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35683643-C-G

139272012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35684007-A-G

139272529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35685010-G-A

http://identifiers.org/hco/5/GRCh38#139272587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35685068-C-A

http://identifiers.org/hco/5/GRCh38#139272731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35685186-C-A

139272731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685186-C-T

139272975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35685375-T-C

139273401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35685811-G-A

139273401-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 35685811-G-C

http://identifiers.org/hco/5/GRCh38#139273447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35685856-C-A

139273467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35685887-G-T

139273539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35685956-A-G

139273644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686054-A-G

139273659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 35686069-G-T

139273675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35686085-T-C

139273739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35686147-G-A

139273823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35686195-A-G

139273823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 35686195-A-T

139274317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686686-G-T

139274440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686798-A-G

139274511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686847-T-C

http://identifiers.org/hco/5/GRCh38#139274549-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35686880-A-C

139274556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686887-T-A

139274556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686887-T-C

139274573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35686904-T-C

139276125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35687482-G-A

139276125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35687482-G-C

139276161-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35687525-C-G

139278311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35689653-T-C

139278383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35689721-T-G

139278435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35689767-T-C

139278435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35689767-T-G

139278490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35689811-A-G

139278529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 35689880-G-A

http://identifiers.org/hco/5/GRCh38#139278565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35689948-A-C

139278808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35690111-A-G

http://identifiers.org/hco/5/GRCh38#139279075-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35690405-C-A

139279075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35690405-C-T

http://identifiers.org/hco/5/GRCh38#139279148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#35690468-A-C

139279148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35690468-A-G

139293388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 35694958-G-T

http://identifiers.org/hco/5/GRCh38#139293422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: http://identifiers.org/mco/18/GRCm39#35694990-C-A

139293492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35695059-T-C

139293492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35695059-T-G

139293503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24624
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 35695070-G-T