http://identifiers.org/hco/6/GRCh38#29956603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449307-C-A

29956603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449307-C-T

29956606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449304-C-T

29956611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449299-A-G

29956616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449294-G-A

http://identifiers.org/hco/6/GRCh38#29956624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449286-C-A

29956624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449286-C-T

29956626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449284-G-A

29956626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449284-G-C

29956626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449284-G-T

29956628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449282-G-A

29956628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449282-G-T

29956629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449281-A-G

29956632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449278-T-C

29956633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449277-G-T

29956635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449275-A-G

29956644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449266-G-A

http://identifiers.org/hco/6/GRCh38#29956652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449258-C-A

29956660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449250-G-A

29956660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449250-G-T

29956664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449246-G-A

http://identifiers.org/hco/6/GRCh38#29956679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449229-C-A

29956679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449229-C-T

29956690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449218-A-T

http://identifiers.org/hco/6/GRCh38#29956692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449216-C-A

29956692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449216-C-T

29956712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449196-G-A

29956712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449196-G-T

http://identifiers.org/hco/6/GRCh38#29956726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449182-C-A

29956726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449182-C-T

29956727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449181-A-G

29956728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449180-G-A

29956728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449180-G-T

29956739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449169-G-A

29956739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449169-G-T

29956758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449147-A-G

29956759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449146-G-T

http://identifiers.org/hco/6/GRCh38#29956786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449133-C-A

29956786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449133-C-T

http://identifiers.org/hco/6/GRCh38#29956790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449129-C-A

29956790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449129-C-T

http://identifiers.org/hco/6/GRCh38#29956791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449128-A-C

29956791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449128-A-G

29956807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449121-G-A

29956808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449120-T-C

29956810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449118-G-A

29956810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449118-G-T

http://identifiers.org/hco/6/GRCh38#29956841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36449088-A-C

29956841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449088-A-G

29956842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449087-G-C

29956842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449087-G-T

29956848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36449081-A-G

29956874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449054-G-A

29956874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449054-G-T

29956875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449053-T-C

29956875-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449053-T-G

29956876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449052-G-A

29956876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36449052-G-T

29956912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448917-T-A

29956934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448887-T-A

29956934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448887-T-C

29956934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448887-T-G

29956939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448882-C-G

29956939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448882-C-T

http://identifiers.org/hco/6/GRCh38#29956962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448863-C-A

29956973-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448849-A-T

29957013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448811-G-A

29957095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448739-T-C

http://identifiers.org/hco/6/GRCh38#29957103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448731-C-A

29957103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448731-C-T

29957123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448712-C-T

29957131-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448704-T-A

29957182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448651-T-C

29957193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448643-G-T

http://identifiers.org/hco/6/GRCh38#29957255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448578-C-A

29957287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448511-A-G

29957295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448503-G-A

29957295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448503-G-T

29957301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448497-G-A

29957301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448497-G-T

29957303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448495-T-C

29957303-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448495-T-G

29957315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448483-G-T

29957322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448476-G-A

29957322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448476-G-T

http://identifiers.org/hco/6/GRCh38#29957324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448474-C-A

29957328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448470-G-A

29957328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448470-G-T

29957329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448469-T-A

29957329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448469-T-C

29957329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448469-T-G

http://identifiers.org/hco/6/GRCh38#29957336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448462-C-A

29957336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448462-C-T

29957338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448460-T-A

29957338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448460-T-C

29957338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448460-T-G

http://identifiers.org/hco/6/GRCh38#29957344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448449-C-A

29957344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448449-C-T

29957349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448444-G-A

29957349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448444-G-T

http://identifiers.org/hco/6/GRCh38#29957405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448387-C-A

29957405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448387-C-G

29957405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448387-C-T

http://identifiers.org/hco/6/GRCh38#29957413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448379-C-A

29957413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448379-C-T

29957414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448378-T-C

29957414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448378-T-G

29957416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448376-A-G

http://identifiers.org/hco/6/GRCh38#29957417-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448375-A-C

29957417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448375-A-G

http://identifiers.org/hco/6/GRCh38#29957425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448367-A-C

29957425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448367-A-G

29957425-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448367-A-T

http://identifiers.org/hco/6/GRCh38#29957431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448361-C-A

29957431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36448361-C-G

29957431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36448361-C-T

http://identifiers.org/hco/6/GRCh38#29957432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448360-C-A

29957432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36448360-C-G

29957432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36448360-C-T

29957448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448343-G-A

29957448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448343-G-T

http://identifiers.org/hco/6/GRCh38#29957450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448341-C-A

http://identifiers.org/hco/6/GRCh38#29957455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448336-A-C

29957455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448336-A-G

29957455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448336-A-T

http://identifiers.org/hco/6/GRCh38#29957460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448331-C-A

29957460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448331-C-T

http://identifiers.org/hco/6/GRCh38#29957462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448329-A-C

29957462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448329-A-G

http://identifiers.org/hco/6/GRCh38#29957467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448324-C-A

29957467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448324-C-G

29957467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448324-C-T

29957471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448320-T-C

29957471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448320-T-G

http://identifiers.org/hco/6/GRCh38#29957480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448311-A-C

29957480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448311-A-G

29957480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448311-A-T

29957482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448309-G-A

29957482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448309-G-T

http://identifiers.org/hco/6/GRCh38#29957487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448304-C-A

29957487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448304-C-G

29957487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448304-C-T

29957497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448294-T-C

29957497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448294-T-G

29957508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448283-G-A

29957508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448283-G-T

29957522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448269-T-A

29957522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448269-T-C

29957522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448269-T-G

29957524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448267-G-T

29957525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448266-A-G

http://identifiers.org/hco/6/GRCh38#29957529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448262-C-A

29957529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448262-C-T

http://identifiers.org/hco/6/GRCh38#29957539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448252-C-A

29957539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448252-C-T

29957540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448251-A-G

29957541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448250-G-A

29957541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448250-G-T

29957542-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448249-T-A

29957542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448249-T-C

29957542-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448249-T-G

29957543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448248-A-G

29957544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448247-G-A

29957544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448247-G-T

29957546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448245-G-A

29957546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448245-G-T

29957548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448243-G-A

29957548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448243-G-C

29957548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448243-G-T

http://identifiers.org/hco/6/GRCh38#29957554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448237-C-A

29957554-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448237-C-G

29957554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448237-C-T

29957557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448234-G-T

http://identifiers.org/hco/6/GRCh38#29957560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448231-C-A

29957560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448231-C-T

29957569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448222-G-T

29957581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448210-G-A

29957581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448210-G-T

29957582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448209-T-G

29957600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448191-G-A

29957600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448191-G-T

29957629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448162-G-A

29957629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448162-G-T

29957630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448161-T-C

29957633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448158-T-C

http://identifiers.org/hco/6/GRCh38#29957639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448152-C-A

29957640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448151-T-C

29957647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448144-G-A

29957647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448144-G-C

29957647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448144-G-T

29957648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448143-A-G

29957648-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448143-A-T

29957649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448142-G-A

29957672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448119-T-A

29957672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448119-T-C

http://identifiers.org/hco/6/GRCh38#29957679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448112-C-A

29957679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448112-C-T

29957680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448111-G-A

29957680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448111-G-C

29957680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448111-G-T

29957683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448108-G-A

29957683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448108-G-C

29957683-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448108-G-T

29957684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448107-G-A

29957684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448107-G-T

29957708-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448083-G-C

29957708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36448083-G-T

29957716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448074-A-G

29957736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448051-T-A

29957736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448051-T-G

29957737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448050-G-A

29957737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448050-G-T

http://identifiers.org/hco/6/GRCh38#29957744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36448049-C-A

29957745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448048-T-A

29957745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448048-T-C

29957747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448046-A-G

29957786-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448009-C-G

29957786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36448009-C-T

29957803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447994-T-C

29957803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447994-T-G

http://identifiers.org/hco/6/GRCh38#29957814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447983-C-A

29957814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447983-C-T

29957816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447981-T-A

29957816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447981-T-C

29957817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447980-C-G

http://identifiers.org/hco/6/GRCh38#29957818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447979-A-C

29957818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447979-A-G

29957822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447966-T-C

29957822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447966-T-G

http://identifiers.org/hco/6/GRCh38#29957823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447965-C-A

29957823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447965-C-G

29957823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447965-C-T

http://identifiers.org/hco/6/GRCh38#29957828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447960-C-A

29957828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447960-C-G

http://identifiers.org/hco/6/GRCh38#29957838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447950-A-C

29957838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 36447950-A-G

29957865-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447929-T-A

29957865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447929-T-C

29957865-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447929-T-G

http://identifiers.org/hco/6/GRCh38#29957866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447928-C-A

http://identifiers.org/hco/6/GRCh38#29957867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447927-A-C

29957867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447927-A-G

29957868-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447926-T-A

29957868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447926-T-C

29957868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447926-T-G

29957869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447925-G-A

29957869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447925-G-C

29957869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447925-G-T

http://identifiers.org/hco/6/GRCh38#29957879-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447915-A-C

29957879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447915-A-G

29957879-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447915-A-T

http://identifiers.org/hco/6/GRCh38#29957884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447910-C-A

29957889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447905-T-C

http://identifiers.org/hco/6/GRCh38#29957908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447883-C-A

29957908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447883-C-T

http://identifiers.org/hco/6/GRCh38#29957910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447881-C-A

29957910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447881-C-T

29957919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447872-T-A

29957919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447872-T-C

29957919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447872-T-G

29957926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447865-T-A

29957926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447865-T-C

29957926-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447865-T-G

29957978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447853-T-C

http://identifiers.org/hco/6/GRCh38#29958217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447567-A-C

29958217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447567-A-G

http://identifiers.org/hco/6/GRCh38#29958220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447564-C-A

29958229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447555-A-G

http://identifiers.org/hco/6/GRCh38#29958243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447541-C-A

29958243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447541-C-T

29958250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447535-G-T

29958330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447470-T-C

29958341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36447459-G-A

29958341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36447459-G-T

29958356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447444-T-C

29958356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447444-T-G

http://identifiers.org/hco/6/GRCh38#29958357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447443-A-C

29958357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447443-A-G

29958363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447437-A-G

29958371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447429-T-A

29958371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447429-T-C

29958371-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447429-T-G

http://identifiers.org/hco/6/GRCh38#29958373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447427-C-A

29958373-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36447427-C-G

29958373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36447427-C-T

29958377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 36447423-T-C

29958377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: 36447423-T-G

http://identifiers.org/hco/6/GRCh38#29958403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447403-C-A

29958403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447403-C-T

29958415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447391-G-A

29958415-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447391-G-T

29958443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447379-A-G

29958477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447353-T-C

29958477-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447353-T-G

29958483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447347-G-A

29958483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447347-G-T

29958485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447345-G-A

29958485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447345-G-T

29958502-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447330-T-A

29958502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447330-T-C

29958502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447330-T-G

http://identifiers.org/hco/6/GRCh38#29958513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447319-C-A

29958513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36447319-C-T

29958520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 36447312-A-G

29958529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447303-A-G

http://identifiers.org/hco/6/GRCh38#29958533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447299-C-A

29958533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447299-C-G

29958533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447299-C-T

http://identifiers.org/hco/6/GRCh38#29958551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#36447281-C-A

29958551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447281-C-T

29958561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447273-T-A

29958561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447273-T-C

29958561-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23425
most severe consequence: non coding transcript exon variant
orthologous variants: 36447273-T-G