49970621-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61806793-T-A

49972954-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61808332-C-G

49978841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61811002-A-G

http://identifiers.org/hco/13/GRCh38#49978895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61811789-C-A

49978895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61811789-C-T

49979574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812407-T-C

49979612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812450-A-G

http://identifiers.org/hco/13/GRCh38#49979622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61812460-C-A

49979622-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812460-C-G

49979622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812460-C-T

49980166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812904-A-G

49980166-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61812904-A-T

49980325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61813063-T-C

49980715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61813325-G-A

http://identifiers.org/hco/13/GRCh38#49980758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61813367-C-A

49980786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61813394-A-G

49983681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61826355-T-C

49985260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827287-G-A

49985260-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827287-G-C

49985266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827293-G-C

49985357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827378-G-A

49985357-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827378-G-C

49985431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61827444-T-C

http://identifiers.org/hco/13/GRCh38#50010567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61840459-C-A

50011649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61841730-T-C

50011846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61841902-T-C

50012068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842112-G-A

50012072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842116-T-C

50012093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842137-A-G

50012093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842137-A-T

50012141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842185-T-G

50012252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842296-T-C

http://identifiers.org/hco/13/GRCh38#50012286-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61842330-A-C

50012393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842437-C-T

50012474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842518-T-C

50012474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61842518-T-G

50013227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61843268-T-C

50013354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61843351-T-C

50014622-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844185-T-A

50014828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844393-G-A

50014828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844393-G-T

50014836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844401-T-C

50014836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844401-T-G

50014854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844415-A-G

50015007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844544-A-T

http://identifiers.org/hco/13/GRCh38#50015062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61844598-C-A

http://identifiers.org/hco/13/GRCh38#50015151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61844622-A-C

50015151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844622-A-G

50015151-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844622-A-T

http://identifiers.org/hco/13/GRCh38#50015160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61844634-A-C

50015160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844634-A-G

50015160-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844634-A-T

50015166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844640-T-A

50015166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844640-T-G

50015208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844697-T-C

50015269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844737-G-A

50015269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844737-G-T

http://identifiers.org/hco/13/GRCh38#50015270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61844738-C-A

50015270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844738-C-T

50015400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844863-A-G

50015485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844954-G-C

50015502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844970-T-C

50015502-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844970-T-G

50015511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844979-G-A

50015511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61844979-G-C

50015538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845006-A-G

50015601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845069-T-C

50015629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845097-G-A

50015629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845097-G-C

50015775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845243-A-G

50015892-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845360-T-G

http://identifiers.org/hco/13/GRCh38#50016148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61845605-C-A

50016148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845605-C-G

50016148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845605-C-T

50016158-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845619-T-A

50016158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845619-T-C

50016209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845653-G-A

50016290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845717-T-A

50016290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845717-T-G

50016341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845766-G-T

50016362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845787-A-G

50016642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61845956-T-C

50016708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61846102-G-A

50016708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61846102-G-T

50016887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61846272-G-A

50016887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61846272-G-T

http://identifiers.org/hco/13/GRCh38#50016953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61846327-C-A

50017010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61846379-T-C

http://identifiers.org/hco/13/GRCh38#50017997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61847174-C-A

50018468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61847737-C-T

50018534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61847801-G-T

50018687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61847936-G-T

50018726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61847963-G-T

http://identifiers.org/hco/13/GRCh38#50019326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61848068-C-A

50019839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61848681-A-G

http://identifiers.org/hco/13/GRCh38#50020091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61848981-C-A

50020091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61848981-C-T

50020316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 61849203-C-G

50022317-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61854665-A-G

50022440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61854731-G-A

50025609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856118-G-A

50025684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856348-C-T

50025776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856440-A-G

50025793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856460-T-C

50025924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856531-C-T

50025932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856539-C-G

50025932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856539-C-T

http://identifiers.org/hco/13/GRCh38#50025974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61856567-A-C

50025974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61856567-A-G

http://identifiers.org/hco/13/GRCh38#50026082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61856641-A-C

50026615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61857166-A-G

50027266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 61857910-A-G

http://identifiers.org/hco/13/GRCh38#50027293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#61857934-C-A

50027293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 61857934-C-T

50027326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 61857966-A-G

50027422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61858087-T-A

50027422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61858087-T-C

50027459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61858124-C-T

50027526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61858178-G-T

50031577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61859123-T-C

http://identifiers.org/hco/13/GRCh38#50031623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61859196-C-A

50031735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61859351-A-G

50031883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61859480-C-T

50033954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61861100-C-T

50034184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61861298-C-T

50043677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61865934-G-A

50043677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61865934-G-T

50043713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61865966-A-G

http://identifiers.org/hco/13/GRCh38#50044618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61866512-C-A

50044618-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866512-C-G

50044618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866512-C-T

50044626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866520-G-A

50044626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866520-G-T

50044647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866541-T-C

50044724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61866618-T-C

http://identifiers.org/hco/13/GRCh38#50044786-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61866673-C-A

50044786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61866673-C-T

50044787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61866687-A-G

50048382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61868097-T-C

http://identifiers.org/hco/13/GRCh38#50048834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61869207-C-A

50048834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61869207-C-G

50049288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869638-T-C

50049389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869731-T-C

50049465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869798-G-T

50049564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61869866-T-C

50061431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61871531-G-A

50067884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61872742-A-G

50068210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61873088-G-T

http://identifiers.org/hco/13/GRCh38#50069025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61873934-C-A

50069330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61874188-G-A

50069720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61874644-T-C

50070283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875147-T-C

http://identifiers.org/hco/13/GRCh38#50070357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61875207-C-A

50070386-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875235-C-G

50070498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875344-G-T

http://identifiers.org/hco/13/GRCh38#50070597-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61875438-C-A

50070597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61875438-C-T

50070703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875520-A-G

50071026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61875961-T-A

50071504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61876371-G-T

50072228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61877346-C-T

50072232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61877349-T-C

50072362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61877457-T-C

50073340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61878445-A-G

50073467-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61878561-T-A

50073501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61878591-T-C

50073827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61878871-G-C

50073885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61878930-T-G

http://identifiers.org/hco/13/GRCh38#50074043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61879084-A-C

50074044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879085-T-C

50074340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879341-C-G

50074370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879377-T-C

50074546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879611-T-C

50074820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879868-G-A

50074866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61879910-G-C

50075071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880154-G-T

50075427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880519-T-C

http://identifiers.org/hco/13/GRCh38#50075635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61880886-C-A

50075635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61880886-C-T

50075680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880931-G-T

50075687-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880938-G-T

50075712-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880963-G-A

50075712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61880963-G-T

50075797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881020-G-T

50075884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881104-A-G

http://identifiers.org/hco/13/GRCh38#50075910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61881130-A-C

50076578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881516-A-T

50076606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881551-T-C

50076606-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881551-T-G

50076962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61881824-T-C

50077670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61882454-T-C

50077949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61882700-T-C

50079095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61883716-C-T

50079292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61883875-C-T

50079922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884437-T-C

50079973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884477-T-G

50080190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61884691-T-C

50080590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885079-G-A

50080854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885363-G-A

50081151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885581-G-A

50081153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885583-C-T

50081186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885596-G-A

50081186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885596-G-C

50081394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885717-C-T

50081424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885722-G-A

50081424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885722-G-T

50081525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885795-G-A

50081525-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885795-G-C

50081690-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61885934-A-T

50081788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886035-C-T

50081850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886094-G-A

50081856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886100-T-C

http://identifiers.org/hco/13/GRCh38#50081865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886109-C-A

50081865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886109-C-T

50081922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886167-C-T

http://identifiers.org/hco/13/GRCh38#50082080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886325-C-A

50082080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886325-C-T

http://identifiers.org/hco/13/GRCh38#50082092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886337-C-A

50082092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61886337-C-T

http://identifiers.org/hco/13/GRCh38#50082189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886418-C-A

http://identifiers.org/hco/13/GRCh38#50082231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886464-C-A

50082235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886469-C-G

50082235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886469-C-T

50082312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886516-G-T

http://identifiers.org/hco/13/GRCh38#50082360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886556-C-A

http://identifiers.org/hco/13/GRCh38#50082393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886601-C-A

50082393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886601-C-T

50082451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886649-A-G

http://identifiers.org/hco/13/GRCh38#50082494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886689-C-A

50082494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886689-C-G

50082494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886689-C-T

http://identifiers.org/hco/13/GRCh38#50082571-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61886763-C-A

50082571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61886763-C-T

50083010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61887018-G-T

50083630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887881-A-G

50083631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887882-G-A

50083678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61887929-T-C

50085541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888556-G-A

50085592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61888615-T-G

50087096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61892899-A-G

50087721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893427-G-T

50087732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893438-G-A

50087732-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61893438-G-C

50088326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895347-T-C

http://identifiers.org/hco/13/GRCh38#50088828-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61895555-A-C

50088895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895619-T-C

50089051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895768-G-A

50089151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61895858-G-A

50089520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896411-G-A

50090082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61896902-A-G

50090476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61897171-C-T

http://identifiers.org/hco/13/GRCh38#50094800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61898442-A-C

50094872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61898618-A-G

50094951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61898681-T-C

50095265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61898939-C-T

50095876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61899371-G-C

50097371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61900849-C-G

http://identifiers.org/hco/13/GRCh38#50097692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61901624-A-C

50097704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901636-A-G

50098086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901940-T-A

50098097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901948-T-C

50098137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61901987-A-G

50098808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61902879-A-T

50119684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61913619-G-A

50120050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61915940-T-C

50120105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61916192-T-C

50123066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61917367-G-A

50123242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61917769-C-T

50123408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61917942-T-C

http://identifiers.org/hco/13/GRCh38#50124166-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61918565-A-C

50124166-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918565-A-G

50124195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918594-C-T

50124300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61918694-G-A

50124300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61918694-G-C

50124304-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 61918698-G-A

50124336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918735-G-A

http://identifiers.org/hco/13/GRCh38#50124420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61918811-C-A

50124429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918820-G-A

50124429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61918820-G-C

50124654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919030-G-C

50124654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919030-G-T

http://identifiers.org/hco/13/GRCh38#50124659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61919035-C-A

50124660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919036-G-A

50124837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919185-C-T

50125148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919373-G-A

50125157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 61919382-G-T

50125478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919711-G-A

http://identifiers.org/hco/13/GRCh38#50125699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61919928-C-A

50125699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919928-C-G

50125699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 13748
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 61919928-C-T