97142262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614638-A-G

97142277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614581-T-C

97142277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614581-T-G

97142282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614576-T-C

97142410-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614335-T-C

http://identifiers.org/hco/6/GRCh38#97142490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24614256-C-A

97142490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614256-C-T

97142539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24614210-T-C

http://identifiers.org/hco/6/GRCh38#97143374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24608308-C-A

97143400-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608282-G-T

97143401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608281-G-A

97143603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608094-A-G

97143610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608087-T-G

97143628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608069-A-G

http://identifiers.org/hco/6/GRCh38#97143672-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24608033-A-C

97143672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24608033-A-G

http://identifiers.org/hco/6/GRCh38#97143714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24607991-C-A

97143714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24607991-C-G

97143798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24607900-A-G

http://identifiers.org/hco/6/GRCh38#97143826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24607855-C-A

97143826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24607855-C-T

97144489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605992-T-C

http://identifiers.org/hco/6/GRCh38#97144566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24605921-C-A

97144614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605875-A-G

97144680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605531-G-C

97144716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605495-G-A

97144716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605495-G-C

97144730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24605478-A-G

97145232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24604645-T-C

97145781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603655-T-C

http://identifiers.org/hco/6/GRCh38#97145803-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24603633-A-C

97145873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603544-G-T

97145874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603543-G-A

http://identifiers.org/hco/6/GRCh38#97146155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24603297-C-A

97146155-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603297-C-G

http://identifiers.org/hco/6/GRCh38#97146208-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24603249-C-A

97146216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603238-T-A

http://identifiers.org/hco/6/GRCh38#97146245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24603210-C-A

97146246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603209-T-C

97146261-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603196-T-A

97146271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603168-G-T

97146346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603100-C-T

http://identifiers.org/hco/6/GRCh38#97146350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24603096-C-A

97146350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603096-C-T

97146372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24603072-A-G

97146489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602980-G-A

97146584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602901-G-T

97146611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602876-G-A

97146611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602876-G-T

97146650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602838-A-T

97146747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602708-G-T

http://identifiers.org/hco/6/GRCh38#97146754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24602701-A-C

97146766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602690-G-T

97146783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602675-G-C

97146783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602675-G-T

97146802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602658-T-A

97146802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602658-T-C

97146803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3 prime UTR variant
orthologous variants: 24602657-A-G

97146841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense variant
orthologous variants: 24602618-C-T

97146986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24602525-A-G

97147110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24602425-G-T

97147146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24602391-C-T

97147314-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24602232-T-A

97147314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24602232-T-C

97147640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24601535-A-G

97147643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24601532-A-G

97147646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24601529-T-C

97147844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24601354-G-A

97149251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24600855-C-T

97149294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24600819-T-A

97149311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24600806-C-T

97149361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24600758-G-A

97149454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 24600671-T-C

http://identifiers.org/hco/6/GRCh38#97149480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24600669-A-C

97149788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600379-T-C

97150034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600139-A-G

http://identifiers.org/hco/6/GRCh38#97150051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24600123-C-A

97150051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600123-C-G

97150051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600123-C-T

97150069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600105-G-T

http://identifiers.org/hco/6/GRCh38#97150113-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24600060-A-C

97150125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600048-T-A

97150133-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600007-T-G

97150138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600002-T-A

97150138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24600002-T-C

http://identifiers.org/hco/6/GRCh38#97150145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24599979-C-A

http://identifiers.org/hco/6/GRCh38#97150170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24599954-A-C

97150170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599954-A-G

http://identifiers.org/hco/6/GRCh38#97150171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24599953-A-C

97150182-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599942-A-T

97150192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599930-G-A

97150192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599930-G-C

97150502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599672-T-C

97150532-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599649-T-A

97150533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599648-T-C

97150587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599599-C-T

97150617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599571-T-C

97150896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599298-C-T

97151024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599269-G-A

97151120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron variant
orthologous variants: 24599179-G-T

http://identifiers.org/hco/6/GRCh38#97151624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24599027-C-A

97151624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24599027-C-G

97151624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24599027-C-T

97151708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24598943-A-T

97151736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 24598915-T-C

97151799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24598852-G-A

97151807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24598844-T-C

97151835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24598816-T-C

97151835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24598816-T-G

97152104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24598568-T-C

97152192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24598487-A-G

97152311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24598233-T-C

97161660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596635-A-G

97161811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596488-A-G

http://identifiers.org/hco/6/GRCh38#97161852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24596447-C-A

97161852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596447-C-T

97161861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596438-G-T

97161878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596421-G-A

97161878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596421-G-C

97161878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596421-G-T

97161889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596410-A-G

97161949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596355-G-A

97161949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596355-G-T

97161959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596345-T-C

97162033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24596268-T-C

97162055-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense variant
orthologous variants: 24596246-T-G

http://identifiers.org/hco/6/GRCh38#97162065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24596236-A-C

http://identifiers.org/hco/6/GRCh38#97162260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24596038-C-A

97162260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24596038-C-T

97162439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595896-C-G

97162822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595533-C-T

97162956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595325-T-C

97163075-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24595187-A-T

97163394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594866-T-C

97163703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24594533-C-G

97164414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593462-G-A

97165008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591742-T-C

http://identifiers.org/hco/6/GRCh38#97165231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24591258-A-C

97165302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24591187-G-A

97165333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24591156-C-T

97165464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24591022-G-A

97165485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590996-A-G

97165532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590956-G-A

97165532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590956-G-T

97166081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590288-T-G

97166130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590239-G-C

97166187-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590184-T-C

97166251-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24590123-G-C

97166547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589979-C-T

97166550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589976-T-A

97166575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589948-G-A

97166643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589895-G-A

97167005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589579-G-C

97167047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589541-C-T

97167147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589451-G-T

97167207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589253-C-T

97167430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589083-C-T

97167511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24589016-G-T

97167625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588909-C-T

97167712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588755-A-T

http://identifiers.org/hco/6/GRCh38#97167731-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588725-C-A

97167731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588725-C-T

http://identifiers.org/hco/6/GRCh38#97167960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588455-C-A

97167969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588438-T-C

97167969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588438-T-G

97167986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588421-T-A

97167986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588421-T-C

http://identifiers.org/hco/6/GRCh38#97167994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588413-C-A

97167994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588413-C-T

97168006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588403-T-A

97168006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588403-T-C

97168009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588401-G-T

97168055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588386-A-G

97168058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588383-A-G

http://identifiers.org/hco/6/GRCh38#97168062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588379-A-C

97168078-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24588363-T-A

97168078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24588363-T-C

97168084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24588357-G-A

97168114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24588327-G-C

97168122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24588319-C-T

97168213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24588228-A-G

97168222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 24588219-C-T

http://identifiers.org/hco/6/GRCh38#97168248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588193-A-C

97168264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588177-C-T

http://identifiers.org/hco/6/GRCh38#97168286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24588156-C-A

97168286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24588156-C-T

97171991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24587455-T-C

97172167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24587217-T-C

97172168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24587216-G-A

97172168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24587216-G-T

97172245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24587131-C-T

97172470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24586901-A-T

97172639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24586743-G-A

97172996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24586403-T-G

97173005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24586394-A-G

http://identifiers.org/hco/6/GRCh38#97173020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24586379-C-A

97173020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24586379-C-T

97173096-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24586307-T-A

97173574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585646-C-T

97173760-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585446-T-A

97173785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585419-A-G

97173794-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585410-T-A

97173794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585410-T-C

97173794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585410-T-G

97173815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585389-G-T

http://identifiers.org/hco/6/GRCh38#97173848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24585369-A-C

97173853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24585364-G-A

http://identifiers.org/hco/6/GRCh38#97173876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24585343-A-C

97175936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584224-G-A

97176143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584039-C-G

97176172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24584011-T-C

97176217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583969-G-T

97176260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24583912-G-A

97176797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582657-T-C

97176884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582572-C-T

http://identifiers.org/hco/6/GRCh38#97177115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24582483-C-A

97177187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582444-A-G

97177324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582318-C-T

97177438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24582209-G-A

97177908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581736-C-T

http://identifiers.org/hco/6/GRCh38#97178296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24581381-C-A

http://identifiers.org/hco/6/GRCh38#97178297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24581380-C-A

97178297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581380-C-T

http://identifiers.org/hco/6/GRCh38#97178300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24581377-C-A

97178300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581377-C-T

97178308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581369-T-C

97178325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581352-A-G

97178384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581291-G-C

97178384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581291-G-T

http://identifiers.org/hco/6/GRCh38#97178424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24581256-A-C

97178424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581256-A-G

97178433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581252-T-C

97178433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581252-T-G

97178474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24581211-T-C

97178534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24581151-A-G

97178617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581067-A-G

97178657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581027-T-C

97178668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24581009-T-C

97178774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580906-C-T

http://identifiers.org/hco/6/GRCh38#97178853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24580659-C-A

97178913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580599-C-T

97179286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580274-G-A

97179286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580274-G-T

http://identifiers.org/hco/6/GRCh38#97179296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24580264-C-A

97179316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580242-T-C

97179327-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580230-A-T

97179329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580228-T-A

97179368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580213-A-G

97179423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24580185-G-C

97179536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24580075-T-C

97179536-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24580075-T-G

97179552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24580059-A-G

97179562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24580049-G-A

97179563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24580048-T-A

97179563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24580048-T-C

http://identifiers.org/hco/6/GRCh38#97179647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24579973-C-A

97179647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579973-C-T

http://identifiers.org/hco/6/GRCh38#97179656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24579963-C-A

97179656-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579963-C-G

97179656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579963-C-T

97179659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579960-T-C

97179659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579960-T-G

http://identifiers.org/hco/6/GRCh38#97179676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24579945-C-A

97179676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579945-C-T

97179806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579827-T-C

97181597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579194-T-C

97181639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579157-G-C

http://identifiers.org/hco/6/GRCh38#97181759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24578981-C-A

97181759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578981-C-T

97181801-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578959-T-A

97181801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578959-T-C

97181846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578921-G-T

97182058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24578747-G-C

97182194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578638-G-A

97182194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578638-G-T

http://identifiers.org/hco/6/GRCh38#97182317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24578534-C-A

97182424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578435-T-C

http://identifiers.org/hco/6/GRCh38#97182494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24578370-A-C

97182949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578018-C-T

97183096-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577914-A-T

97186487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24574582-T-A

97186487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24574582-T-G

97186592-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24574477-A-T

97186714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574355-T-C

97186714-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574355-T-G

97186742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574329-T-C

97186825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574241-T-C

97187566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573529-T-C

97187566-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573529-T-G

http://identifiers.org/hco/6/GRCh38#97187631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24573456-A-C

97187631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573456-A-G

97187695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573371-T-C

97188240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572258-T-C

97188241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572257-G-C

97188261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572234-A-G

97188394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572124-G-A

http://identifiers.org/hco/6/GRCh38#97189166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24569412-C-A

97189952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569020-G-A

97190434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568645-T-C

97190630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568459-T-C

97190847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568254-C-G

97190891-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568228-T-A

97191040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568117-G-C

97191200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568032-G-A

97191200-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568032-G-C

97191215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568017-G-C

http://identifiers.org/hco/6/GRCh38#97191217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24568015-A-C

97191515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567830-T-C

97191607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567730-T-A

97191607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567730-T-C

97192073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567139-T-C

97192088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567124-C-T

97192263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24567036-G-A

97192348-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566958-A-T

97192362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566944-C-T

97192874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566392-T-A

97193014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566271-T-C

97193245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566073-T-A

97194518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24565138-T-C

97194669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564947-G-A

97194687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564933-C-T

97194910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564727-T-C

97194910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564727-T-G

97194930-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564710-C-G

97194935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564705-A-G

97194990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564649-C-T

97195143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564594-T-C

97195183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564554-G-A

97195183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564554-G-C

97195201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564534-A-T

97195284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564460-T-C

97195406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24564351-A-G

97197204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562231-C-T

97197248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562174-A-G

97197379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24562041-T-C

http://identifiers.org/hco/6/GRCh38#97197503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24561915-C-A

http://identifiers.org/hco/6/GRCh38#97199000-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24561411-A-C

97199250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561177-T-C

97199350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24561077-T-C

97199622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560803-T-C

97199622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560803-T-G

97199675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560754-C-T

97199687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560742-C-T

http://identifiers.org/hco/6/GRCh38#97199761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24560681-A-C

97199761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24560681-A-G

http://identifiers.org/hco/6/GRCh38#97199903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24560547-A-C

97200573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24559922-T-C

97200587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24559908-C-G

97200628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24559856-C-G

97201151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24559050-A-G

http://identifiers.org/hco/6/GRCh38#97201174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24559039-A-C

97201253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24558975-G-A

97201380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 24558850-C-T

http://identifiers.org/hco/6/GRCh38#97201722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24558510-A-C

97201830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558404-A-G

97202004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558232-G-C

97202062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558174-A-T

97202109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558130-A-G

97202314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557689-G-A

97202356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557647-A-G

97202356-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557647-A-T

97202401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557295-A-G

97202456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557245-T-C

97202463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557238-G-A

97202463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557238-G-C

97202476-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557225-T-A

97202476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557225-T-C

97202509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557192-A-G

97202509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557192-A-T

97202650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557060-C-T

97202848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557003-T-C

http://identifiers.org/hco/6/GRCh38#97202960-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24556895-C-A

http://identifiers.org/hco/6/GRCh38#97203179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24556693-C-A

97203179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556693-C-G

97203682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556163-T-C

97203682-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556163-T-G

http://identifiers.org/hco/6/GRCh38#97203862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24555970-A-C

97203866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555966-T-A

97203867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555965-T-C

97204281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555611-A-G

97204494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555414-T-G

97204514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555397-G-T

97205483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555187-C-T

http://identifiers.org/hco/6/GRCh38#97206822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24553802-C-A

97207185-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553469-T-A

97207256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553379-G-A

97207308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553334-T-C

97207429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553226-C-G

97207474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553163-A-G

97207654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552987-C-G

97207830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552819-T-C

97207921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552756-G-A

97207932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552745-C-T

97207947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552730-G-C

97208072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552489-C-T

97208136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552430-T-A

97208308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552230-C-T

97210976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24550480-T-C

http://identifiers.org/hco/6/GRCh38#97211065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24550410-A-C

97211478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549786-C-T

http://identifiers.org/hco/6/GRCh38#97211544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24549725-A-C

97211874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549414-T-G

97211960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549342-A-T

97212413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548926-G-A

97212490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548846-T-C

97212946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548273-T-C

97212979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548235-T-A

97213058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548138-T-C

97213216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547988-G-A

97213925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546581-A-T

97214338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546131-T-C

97214340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546129-T-C

97214501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545790-A-G

97214603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545708-T-C

97214753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545575-T-G

97214830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545490-A-T

97215126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545208-C-T

97216361-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543957-C-G

97216579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543788-T-C

97216836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543573-T-G

97217182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24543250-C-T

97218221-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542909-T-A

http://identifiers.org/hco/6/GRCh38#97218332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24542801-C-A

97218332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542801-C-T

97218347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542786-T-C

97218500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542632-C-T

97218551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542592-T-C

97219329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542375-T-C

97219731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541789-T-C

97219861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541670-T-C

97219928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541601-T-C

http://identifiers.org/hco/6/GRCh38#97219967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24541568-C-A

http://identifiers.org/hco/6/GRCh38#97220055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24541486-C-A

97221249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24540706-A-G

97221586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24540441-G-T

http://identifiers.org/hco/6/GRCh38#97221738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24540273-C-A

97221738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24540273-C-T

97222076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539957-C-T

http://identifiers.org/hco/6/GRCh38#97222406-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24539430-A-C

97222420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539416-C-T

97222571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539262-C-T

http://identifiers.org/hco/6/GRCh38#97222748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24539086-A-C

97222944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538893-T-G

97223062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538777-A-G

97223115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538724-G-C

97223406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538410-C-T

97223460-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538349-G-C

97223460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538349-G-T

97223606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538209-A-G

http://identifiers.org/hco/6/GRCh38#97223742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24538095-C-A

97224103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24537607-T-C

97224111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24537599-G-A

97224157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24537548-A-G

97224192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24537509-G-T

http://identifiers.org/hco/6/GRCh38#97224206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24537498-A-C

97228174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24536708-C-T

97228228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24536659-T-C

http://identifiers.org/hco/6/GRCh38#97228749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24536536-C-A

97228749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24536536-C-G

97228749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24536536-C-T

97228779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24536509-T-C

97229189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24536151-C-T

97229269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24536071-A-T

97229476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24535873-T-C

97229894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534868-G-A

97230478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534608-T-C

97230558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534530-T-C

http://identifiers.org/hco/6/GRCh38#97230940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24534188-C-A

97230940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534188-C-G

97230953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534174-G-T

97231037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534063-G-A

97231037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534063-G-T

97231039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534061-G-A

97231039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534061-G-T

97231043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534057-G-A

97231043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24534057-G-T

97231401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24533158-T-A

97231456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24533097-C-T

97231463-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24533090-T-A

http://identifiers.org/hco/6/GRCh38#97231481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24533072-C-A

97231481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24533072-C-T

97231554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24532999-G-A

97231554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 24532999-G-T

97231775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24532801-C-T

97231777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24532799-T-A

97231777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24532799-T-C

97231849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24532727-C-T

97232349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530661-T-C

97232758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530399-A-G

97233114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530101-G-A

97233212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530025-G-A

97233213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530024-G-A

97233222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24530016-T-C

97233259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529986-T-C

http://identifiers.org/hco/6/GRCh38#97233550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24529718-C-A

97233550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529718-C-G

97233618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529396-C-T

http://identifiers.org/hco/6/GRCh38#97233727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24529285-C-A

http://identifiers.org/hco/6/GRCh38#97233789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24529229-C-A

97233789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529229-C-G

97233796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529223-G-C

97233796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529223-G-T

97233849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24529173-C-T

97234037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24528988-T-C

97234282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24528769-A-G

97234317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24528738-T-A

97234317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24528738-T-C

97245884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24522036-C-T

97245887-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24522033-A-T

97245923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521997-A-G

97246181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521754-A-G

97246608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521321-G-A

http://identifiers.org/hco/6/GRCh38#97246610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24521319-C-A

97246616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521313-T-A

97246741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521188-A-G

97246770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521167-G-C

97246770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521167-G-T

97246870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521078-T-C

97246919-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24521028-T-G

97246983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24520971-A-T

97247246-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24520639-T-G

97247379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24520530-T-G

97251416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24519140-C-T

97254210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24517527-G-T

97254268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24517470-G-A

97254269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24517469-A-G

97254282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24517456-A-G

http://identifiers.org/hco/6/GRCh38#97254290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24517448-A-C

97254657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24517134-G-A

97256340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24516072-A-G

97256506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24515805-T-C

97256506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24515805-T-G

http://identifiers.org/hco/6/GRCh38#97257763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24515108-A-C

97257763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24515108-A-G

97257825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24515046-C-T

97258049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24514799-C-T

97258288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24514555-A-G

97258288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24514555-A-T

97258323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24514524-T-C

97258345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24514502-T-C

97258745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24514174-T-C

97258861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24513933-A-G

97258955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24513850-G-T

97259004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24513801-A-G

97263459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24508392-T-C

97263481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24508375-A-G

http://identifiers.org/hco/6/GRCh38#97263500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24508364-A-C

http://identifiers.org/hco/6/GRCh38#97263517-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24508347-A-C

97263517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24508347-A-T

97267812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24507493-A-G

97267929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 24507385-T-C

97267929-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24507385-T-G

97268072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507241-A-G

97268072-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507241-A-T

97268083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507230-A-G

97268111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507205-A-G

97268111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507205-A-T

97268118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24507198-T-C

97269570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24506243-G-A

97270207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24505154-G-T

97270257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24505104-T-C

97270257-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24505104-T-G

97270273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24505088-T-C

97270370-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504930-T-G

97270371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504929-A-G

http://identifiers.org/hco/6/GRCh38#97270426-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24504878-C-A

97270426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504878-C-T

97270684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504672-A-G

97270718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504641-T-C

97270721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504638-G-A

97270771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504596-T-C

97270796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24504571-A-G

97271139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503968-G-A

97271139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503968-G-T

97271264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503720-T-C

97271327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503659-T-C

97272412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503357-G-A

http://identifiers.org/hco/6/GRCh38#97272510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24503257-C-A

http://identifiers.org/hco/6/GRCh38#97272585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24503210-C-A

97272604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503201-C-G

97272609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24503196-G-T

97272841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24502973-G-A

97273020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24502788-T-C

97275849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501386-T-C

97275880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501357-G-A

97275985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501266-T-C

97276001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501250-C-T

97276033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501218-A-G

97276118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24501104-A-T

97278913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24500020-G-A

http://identifiers.org/hco/6/GRCh38#97278966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24499968-C-A

http://identifiers.org/hco/6/GRCh38#97278995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24499940-C-A

97278995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24499940-C-T

97279089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24499852-T-C

97279130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24499817-A-G

http://identifiers.org/hco/6/GRCh38#97281114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24498068-C-A

97281114-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24498068-C-G

97281114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24498068-C-T

97281134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24498044-T-C

97281456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497790-A-G

97281456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497790-A-T

97281738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497553-A-G

97281745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497546-G-A

97281764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497528-T-C

97282096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497208-G-T

97282271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 24497110-G-C

97282416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 24496967-G-A

http://identifiers.org/hco/6/GRCh38#97282510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24496868-C-A

97282510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496868-C-T

97282520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496858-T-C

97282520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496858-T-G

http://identifiers.org/hco/6/GRCh38#97282522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24496857-A-C

97282522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496857-A-G

97282528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496851-T-A

97282528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496851-T-C

97282528-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 24496851-T-G

http://identifiers.org/hco/6/GRCh38#97283194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#24496443-C-A

97283194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496443-C-T

97283227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, undefined
orthologous variants: 24496426-G-C

97283227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: intron_variant, undefined
orthologous variants: 24496426-G-T

97283367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496326-T-A

97283386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496306-T-C

97283386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496306-T-G

97283388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496304-G-A

97283410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496296-G-A

97283410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496296-G-T

97283423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 24496283-A-G

http://identifiers.org/hco/6/GRCh38#97283465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#24496239-C-A

97283466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24496238-A-G

97283524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24496202-C-G

97283524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21475
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 24496202-C-T