15564081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725877-G-A

15564081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725877-G-T

http://identifiers.org/hco/19/GRCh38#15564087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32725883-C-A

15564087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725883-C-T

15564104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725900-T-C

15564104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725900-T-G

15564145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725941-G-A

15564145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32725941-G-T

15564212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32726008-G-A

15564212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32726008-G-T

15564363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726133-G-A

15564363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726133-G-T

15564384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726142-G-A

15564384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32726142-G-T

15565924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735512-G-T

15566304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735709-G-A

15566411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735750-A-G

15566473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735807-C-T

15566569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32735909-C-T

15571566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736685-G-A

15571604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736723-A-G

15571604-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736723-A-T

15571627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736765-G-T

15571630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736768-A-G

15571630-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736768-A-T

15571635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736773-T-C

15571636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736774-G-A

15571636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736774-G-T

15571646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736784-G-A

15571646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32736784-G-T

http://identifiers.org/hco/19/GRCh38#15571823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32736957-C-A

15571823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32736957-C-T

15571890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737026-A-G

15571958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737089-T-C

15571961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737092-G-A

15571961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737092-G-C

15571961-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737092-G-T

http://identifiers.org/hco/19/GRCh38#15571988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32737122-A-C

http://identifiers.org/hco/19/GRCh38#15572007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32737136-C-A

15572007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737136-C-T

15572010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32737139-G-T

15572822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32738962-T-C

15572829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32738974-G-A

15572893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739020-G-C

http://identifiers.org/hco/19/GRCh38#15573406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739148-C-A

15573406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739148-C-T

15573499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739238-G-A

15573499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739238-G-T

http://identifiers.org/hco/19/GRCh38#15573506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739245-C-A

15573506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739245-C-T

http://identifiers.org/hco/19/GRCh38#15573512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739251-C-A

15573512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739251-C-T

http://identifiers.org/hco/19/GRCh38#15573582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739326-A-C

15573582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739326-A-G

15573582-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739326-A-T

http://identifiers.org/hco/19/GRCh38#15573596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739340-C-A

15573596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32739340-C-T

15573618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32739362-T-C

15573618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32739362-T-G

15573659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739403-A-G

15573700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739441-T-C

http://identifiers.org/hco/19/GRCh38#15573707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739448-C-A

15573707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739448-C-T

15573715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739456-T-C

15573715-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739456-T-G

15573728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739468-C-T

http://identifiers.org/hco/19/GRCh38#15573817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32739556-C-A

15573817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32739556-C-T

15573869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32739608-A-G

http://identifiers.org/hco/19/GRCh38#15575070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32740351-C-A

15575138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740473-T-A

15575574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740939-G-A

15575574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740939-G-T

15575624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740997-T-G

http://identifiers.org/hco/19/GRCh38#15575626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32740999-C-A

15575626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32740999-C-T

15575628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741001-G-A

15575628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741001-G-C

15575628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741001-G-T

15575739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32741117-A-G

15575740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32741118-G-A

15575751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32741129-G-A

15575751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32741129-G-T

15575819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32741197-G-A

15575866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32741243-G-A

15576261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742593-G-A

15576392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32742769-T-C

http://identifiers.org/hco/19/GRCh38#15576658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743069-C-A

15576658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743069-C-T

15576686-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743097-T-A

15576686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743097-T-C

15576763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743174-T-C

http://identifiers.org/hco/19/GRCh38#15576882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743293-C-A

15576882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743293-C-T

http://identifiers.org/hco/19/GRCh38#15577058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743439-C-A

15577113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743493-T-C

15577133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743513-T-C

http://identifiers.org/hco/19/GRCh38#15577229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743609-C-A

15577229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743609-C-G

15577229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743609-C-T

http://identifiers.org/hco/19/GRCh38#15577249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743629-C-A

15577249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743629-C-T

15577327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743703-A-G

15577330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743706-T-C

http://identifiers.org/hco/19/GRCh38#15577333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743709-C-A

15577343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743719-T-C

15577360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743738-A-G

http://identifiers.org/hco/19/GRCh38#15577371-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743749-C-A

15577371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743749-C-T

15577401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743779-G-T

http://identifiers.org/hco/19/GRCh38#15577409-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743787-A-C

15577409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743787-A-G

15577409-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743787-A-T

15577412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743790-T-C

15577412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743790-T-G

15577427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32743805-T-A

15577427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32743805-T-C

15577427-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32743805-T-G

http://identifiers.org/hco/19/GRCh38#15577441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743819-C-A

15577441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743819-C-T

15577452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743830-G-A

15577452-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743830-G-T

15577480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743858-G-A

15577480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743858-G-T

15577489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743867-A-G

15577489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743867-A-T

http://identifiers.org/hco/19/GRCh38#15577508-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743886-C-A

15577508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743886-C-T

http://identifiers.org/hco/19/GRCh38#15577522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743900-A-C

15577522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743900-A-G

15577536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743914-A-G

15577546-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743924-T-A

15577546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743924-T-C

http://identifiers.org/hco/19/GRCh38#15577547-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32743925-A-C

15577547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32743925-A-G

15577563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743941-G-A

15577563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743941-G-C

15577563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743941-G-T

15577567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32743945-G-A

15577567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32743945-G-T

15577577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743959-T-C

15577577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743959-T-G

15577579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743961-A-G

15577579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32743961-A-T

15582950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32745831-A-G

15583311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746776-T-A

15583311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746776-T-C

15583311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746776-T-G

http://identifiers.org/hco/19/GRCh38#15583320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32746785-C-A

15583320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746785-C-T

15583334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746799-T-A

15583334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746799-T-C

15583335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32746800-T-C

15583368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746833-G-A

15583368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746833-G-C

15583368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746833-G-T

15583404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746869-G-A

15583404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746869-G-C

15583404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746869-G-T

http://identifiers.org/hco/19/GRCh38#15583421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32746886-C-A

15583421-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746886-C-G

15583421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746886-C-T

15583450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746915-G-A

15583450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746915-G-C

15583450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32746915-G-T

15583561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747004-T-C

15583647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747088-G-A

15583647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747088-G-T

15583662-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747103-T-A

15583662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747103-T-C

15583662-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747103-T-G

15583713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747154-A-G

15584125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747251-T-A

15584125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747251-T-C

15584125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747251-T-G

http://identifiers.org/hco/19/GRCh38#15584198-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747324-A-C

15584198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747324-A-G

15584198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747324-A-T

http://identifiers.org/hco/19/GRCh38#15584204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747330-C-A

15584204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747330-C-G

15584204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747330-C-T

http://identifiers.org/hco/19/GRCh38#15584234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747351-C-A

15584234-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747351-C-G

15584234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747351-C-T

http://identifiers.org/hco/19/GRCh38#15584262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747391-C-A

15584262-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747391-C-G

15584262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747391-C-T

15584266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747395-G-A

15584266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747395-G-T

15584298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747438-T-A

15584298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747438-T-C

15584298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747438-T-G

http://identifiers.org/hco/19/GRCh38#15584320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747457-A-C

15584320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747457-A-G

15584320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747457-A-T

15584329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747477-G-T

15584336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747484-T-C

15584401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747539-G-A

15584401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747539-G-T

http://identifiers.org/hco/19/GRCh38#15584456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747595-A-C

15584456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747595-A-G

http://identifiers.org/hco/19/GRCh38#15584464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747602-C-A

15584464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747602-C-T

15584498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747630-G-A

15584498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747630-G-C

15584498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32747630-G-T

http://identifiers.org/hco/19/GRCh38#15584542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747671-C-A

15584542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32747671-C-T

http://identifiers.org/hco/19/GRCh38#15584553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747685-C-A

15584553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747685-C-T

15584589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747721-T-A

15584589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747721-T-C

15584589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747721-T-G

http://identifiers.org/hco/19/GRCh38#15584604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747736-C-A

15584604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747736-C-G

15584604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747736-C-T

15584616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747748-G-A

15584616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747748-G-C

15584616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747748-G-T

http://identifiers.org/hco/19/GRCh38#15584617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747749-C-A

15584617-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747749-C-G

15584617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non coding transcript exon variant
orthologous variants: 32747749-C-T

15584652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747784-G-A

15584652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747784-G-T

http://identifiers.org/hco/19/GRCh38#15584655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#32747787-C-A

15584655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747787-C-T

15584685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747817-G-A

15584685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747817-G-C

15584685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39944
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 32747817-G-T