11956390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111709534-G-T

http://identifiers.org/hco/11/GRCh38#11956581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111709702-A-C

11956885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111709993-G-T

11956949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710063-C-T

11957610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710687-T-C

http://identifiers.org/hco/11/GRCh38#11958053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111710877-C-A

11958105-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710919-T-G

http://identifiers.org/hco/11/GRCh38#11958126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111710940-C-A

11958126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111710940-C-T

11958257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711064-C-T

11958259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711066-G-A

11958355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711142-A-T

11958403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711189-G-A

11958540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711277-G-T

11958567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711303-T-C

http://identifiers.org/hco/11/GRCh38#11958596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711330-C-A

11958596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711330-C-T

11958718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711443-G-T

11958724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711449-G-T

11958751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711473-G-C

11958751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711473-G-T

11958756-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711478-G-T

http://identifiers.org/hco/11/GRCh38#11958781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711503-C-A

11958781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711503-C-T

11958938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711668-A-G

11959078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711783-G-T

11959121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111711811-T-C

http://identifiers.org/hco/11/GRCh38#11959169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111711862-C-A

11959169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111711862-C-T

11959196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111711889-C-T

11959291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111711958-T-C

11959384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111712050-A-G

11959390-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111712056-C-G

11959519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3 prime UTR variant
orthologous variants: 111712154-A-G

http://identifiers.org/hco/11/GRCh38#11963262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111716436-C-A

11963323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716499-C-T

http://identifiers.org/hco/11/GRCh38#11963350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111716526-C-A

11963408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716584-A-G

11963422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716598-A-G

11963465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716643-T-C

http://identifiers.org/hco/11/GRCh38#11963550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111716694-C-A

11963550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716694-C-T

11963639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716754-T-C

11963646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716761-A-G

11963646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716761-A-T

11963649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716764-G-T

11963666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716796-T-C

http://identifiers.org/hco/11/GRCh38#11963694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111716823-C-A

11963694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716823-C-T

11963723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716853-C-T

11963880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716915-T-C

http://identifiers.org/hco/11/GRCh38#11963928-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111716960-C-A

11963928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716960-C-G

11963968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111716993-A-G

http://identifiers.org/hco/11/GRCh38#11963980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111717005-C-A

11964023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717034-G-C

11964023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717034-G-T

11964061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717071-T-C

11964076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717085-G-A

11964076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717085-G-T

11964245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717227-T-C

11964247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717229-A-T

11964248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717230-A-G

http://identifiers.org/hco/11/GRCh38#11964261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111717243-C-A

11964261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717243-C-T

11964304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717266-A-G

11964304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717266-A-T

11964353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717315-T-G

11964463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111717417-T-C

11964488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111717442-T-C

11964493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 111717447-C-T

11964572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111717523-C-T

11964724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 111717689-G-T

http://identifiers.org/hco/11/GRCh38#11964745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111717725-C-A

11964766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111717743-G-A

http://identifiers.org/hco/11/GRCh38#11964826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111717801-C-A

11964826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111717801-C-T

http://identifiers.org/hco/11/GRCh38#11965657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111718395-C-A

11965670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718408-T-C

11965685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718423-T-A

11965685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718423-T-C

http://identifiers.org/hco/11/GRCh38#11965719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111718462-C-A

11965784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718530-G-A

11965802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111718548-G-A

11965868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111718614-C-T

11965925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111718671-G-A

11965925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111718671-G-T

11965934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111718680-G-A

11966223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718894-G-A

11966244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718916-G-A

11966244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718916-G-T

11966344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111718988-G-A

11966373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719015-G-C

11966400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719037-G-A

11966484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719117-C-G

11966484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719117-C-T

11966567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719197-G-T

11966569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719199-G-A

11966569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719199-G-C

11966569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719199-G-T

11966777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719430-G-A

11966777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719430-G-T

11966823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719469-A-G

11966870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719506-G-T

11966873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719509-G-A

11966873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719509-G-T

11967127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719768-C-T

11967163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719800-G-T

http://identifiers.org/hco/11/GRCh38#11967196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111719848-C-A

11967196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719848-C-T

11967198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719850-T-C

http://identifiers.org/hco/11/GRCh38#11967201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111719853-C-A

11967213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719869-A-G

11967280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719924-T-C

11967309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719954-C-G

11967309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111719954-C-T

http://identifiers.org/hco/11/GRCh38#11967451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111720088-A-C

11967451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720088-A-G

11967592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720212-T-C

11967608-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720226-G-C

11967934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720493-C-G

11967939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720498-G-T

11968290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720705-G-A

11968290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720705-G-T

http://identifiers.org/hco/11/GRCh38#11968344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111720763-C-A

11968344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720763-C-T

11968366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111720767-C-T

11968437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111720839-G-A

11968502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111720907-A-G

11968567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111720971-G-A

11968567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111720971-G-C

11968567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111720971-G-T

11968600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111720996-A-G

11968607-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111721003-T-A

http://identifiers.org/hco/11/GRCh38#11968621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111721017-C-A

11968621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111721017-C-T

11968677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111721081-G-A

11968677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111721081-G-T

http://identifiers.org/hco/11/GRCh38#11968681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111721085-A-C

http://identifiers.org/hco/11/GRCh38#11968715-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111721131-A-C

11968715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111721131-A-T

11968783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721194-G-A

11968783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721194-G-T

11968840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721249-G-A

11968840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721249-G-T

11968893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721303-T-C

11968893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721303-T-G

11969358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721588-C-T

11969592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721800-C-G

11969719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111721925-G-A

http://identifiers.org/hco/11/GRCh38#11970242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111723220-C-A

11970249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111723227-C-T

11972626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111723339-C-G

11972690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111723383-G-A

11972700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111723391-G-A

11973543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725096-C-T

11973764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725278-G-A

11973880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725401-G-A

11973891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111725408-C-T

11976150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726247-A-G

11976150-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726247-A-T

11976170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726267-G-C

11976203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726298-A-G

11976367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726436-A-T

11976411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726537-C-T

http://identifiers.org/hco/11/GRCh38#11976420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111726546-A-C

11976425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726551-C-G

11976645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111726747-A-G

11976804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111727049-A-G

http://identifiers.org/hco/11/GRCh38#11977214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111727505-C-A

11977214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111727505-C-G

11979113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728012-G-A

11979113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728012-G-T

11979140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728038-T-A

11979140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728038-T-C

11979156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728051-G-C

11979161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728056-T-A

11979161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728056-T-C

11979276-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728141-T-C

11979489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728303-G-A

11979533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728350-C-T

11979560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111728376-G-A

11979609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728416-G-T

11979628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111728445-T-C

11979636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111728456-G-T

11979679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111729102-G-A

11979679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111729102-G-C

11979739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111729148-G-A

11979739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 111729148-G-T

11979895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111729299-A-G

11979928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111729331-G-A

11979928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111729331-G-T

http://identifiers.org/hco/11/GRCh38#11979957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111729362-C-A

http://identifiers.org/hco/11/GRCh38#11980045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111729447-C-A

11980045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111729447-C-T

11980051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111729453-T-C

11980476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111729829-A-G

11980534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111729885-A-G

11984803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111731341-T-C

11984837-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111731359-C-G

11985040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111731554-G-A

11985736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111731703-A-G

11986101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732010-C-T

11986212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732123-A-G

11986278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732185-C-T

11986324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732228-T-C

11986494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732621-C-T

http://identifiers.org/hco/11/GRCh38#11986760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111732908-C-A

11986760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732908-C-T

11986761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732909-G-A

11986762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111732910-G-T

11987069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111734551-T-A

11987451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111734916-G-A

http://identifiers.org/hco/11/GRCh38#11988270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111735982-C-A

11988347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736056-T-C

http://identifiers.org/hco/11/GRCh38#11988480-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111736179-A-C

11988561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736245-A-G

11988581-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736268-T-A

11988581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736268-T-C

11988583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736270-G-A

11988922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111736383-C-T

11990174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111737855-G-A

11990192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111737874-C-T

11990292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111737965-G-A

11990806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111738417-T-C

http://identifiers.org/hco/11/GRCh38#11990860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111738468-C-A

11990860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111738468-C-T

11992116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111739674-C-T

11992273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111739840-C-T

11992284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111739851-T-C

11992298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111739865-C-T

http://identifiers.org/hco/11/GRCh38#11992395-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111739931-C-A

11992569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111740146-T-C

11992577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111740154-C-T

11992617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111740171-G-A

11994192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111742522-G-T

http://identifiers.org/hco/11/GRCh38#11994533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111742790-C-A

11994533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111742790-C-T

http://identifiers.org/hco/11/GRCh38#11994563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111742820-C-A

11994677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111743329-G-A

11994677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111743329-G-T

11994706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111743368-T-C

11994765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743419-G-A

11994765-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743419-G-T

11994933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743597-G-A

11994990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743654-C-T

11995065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743740-T-C

http://identifiers.org/hco/11/GRCh38#11995517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111743841-C-A

11995517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111743841-C-T

11995808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111744107-G-A

11995859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111744158-G-A

11996017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111744311-G-A

11996211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111744482-G-A

11996211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111744482-G-T

11996678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745530-G-T

11996720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745574-G-A

11996720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745574-G-T

11996799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745650-T-C

11997083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111745919-G-A

11997189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746034-C-G

11997189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746034-C-T

http://identifiers.org/hco/11/GRCh38#11997192-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111746037-A-C

11997197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746042-G-A

11997197-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746042-G-T

11997293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746117-T-C

11997335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746150-A-G

11997367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746184-C-G

11997367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111746184-C-T

11997464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747060-C-G

11997464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747060-C-T

11997581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747161-G-A

11997589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747169-T-C

11997606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747189-G-A

http://identifiers.org/hco/11/GRCh38#11997966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111747525-C-A

11997966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747525-C-T

11998054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747569-G-A

11998082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747594-C-T

11998090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747602-T-C

11998108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111747619-C-T

11998235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111747718-G-A

11998235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111747718-G-T

http://identifiers.org/hco/11/GRCh38#11998369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111747836-C-A

11998369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111747836-C-T

http://identifiers.org/hco/11/GRCh38#11998511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111747996-C-A

11998511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111747996-C-T

11998561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748031-G-A

11998561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748031-G-C

http://identifiers.org/hco/11/GRCh38#11998566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111748036-C-A

http://identifiers.org/hco/11/GRCh38#11998605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111748083-C-A

11998605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748083-C-T

11998608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748086-T-C

11998608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748086-T-G

11998669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748144-G-A

11998669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748144-G-T

http://identifiers.org/hco/11/GRCh38#11998689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111748161-A-C

http://identifiers.org/hco/11/GRCh38#11998702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111748174-C-A

11998749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748221-A-G

11998752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111748224-C-T

11998850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748316-G-A

11998850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748316-G-T

11998920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748368-T-C

11998987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748420-G-C

11998997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748430-T-C

11999055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748485-A-G

11999077-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111748503-G-T

12002087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749623-T-C

12002092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749628-T-A

12002204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 111749742-T-C

12002204-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 111749742-T-G

12002205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111749743-T-A

12002205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111749743-T-C

12002205-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 111749743-T-G

http://identifiers.org/hco/11/GRCh38#12002214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111749752-C-A

12002214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749752-C-T

http://identifiers.org/hco/11/GRCh38#12002232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111749757-C-A

12002232-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749757-C-G

12002232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749757-C-T

12002269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749780-T-C

12002389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111749907-C-T

12002468-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111749978-T-A

12002468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111749978-T-C

12002534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750044-A-G

12002539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750049-G-T

12002563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750067-T-C

12002602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750101-G-A

12002602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750101-G-T

12002815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750847-G-A

12002989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111750998-T-C

12003038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111751022-C-T

12003214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111751199-G-C

12003218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111751203-G-T

12003511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111751460-C-T

12003583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111751528-C-T

12004266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753021-C-T

12004460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753152-A-G

12004476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753169-A-T

12004793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753441-T-C

12004868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753501-T-C

12005057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753665-A-G

12005070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111753678-G-T

12005502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754405-T-C

http://identifiers.org/hco/11/GRCh38#12005773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111754666-A-C

12005780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111754673-G-A

12005949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755237-T-C

12006450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755648-G-A

12006604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755786-C-T

12006680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755847-G-A

12006680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755847-G-C

12006692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755860-T-C

12006692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111755860-T-G

12006863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756040-G-A

12007187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756330-A-G

12007704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756692-T-G

12007895-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756886-C-G

12007941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111756925-A-G

12008192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757178-G-C

12008276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757262-G-A

12008276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757262-G-C

12008276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757262-G-T

12008305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757313-T-C

12008310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757318-A-G

12008342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757362-G-A

12008342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757362-G-T

http://identifiers.org/hco/11/GRCh38#12008366-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757386-C-A

http://identifiers.org/hco/11/GRCh38#12008379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757399-C-A

12008379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757399-C-T

12008382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757402-G-T

http://identifiers.org/hco/11/GRCh38#12008475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757495-C-A

12008475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757495-C-G

12008475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757495-C-T

12008503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757523-G-A

12008503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757523-G-C

12008503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757523-G-T

12008523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757543-G-A

12008523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757543-G-T

12008529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757549-G-A

12008529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 111757549-G-C

http://identifiers.org/hco/11/GRCh38#12008575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757595-C-A

12008575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757595-C-T

http://identifiers.org/hco/11/GRCh38#12008588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757608-C-A

http://identifiers.org/hco/11/GRCh38#12008593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757613-C-A

12008593-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757613-C-T

http://identifiers.org/hco/11/GRCh38#12008603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757620-C-A

12008603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757620-C-T

http://identifiers.org/hco/11/GRCh38#12008624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757641-C-A

12008624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757641-C-T

http://identifiers.org/hco/11/GRCh38#12008683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757692-C-A

12008683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757692-C-G

12008739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757720-A-G

12008739-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757720-A-T

http://identifiers.org/hco/11/GRCh38#12008825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757808-C-A

12008825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 111757808-C-T

http://identifiers.org/hco/11/GRCh38#12008852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757834-C-A

12008889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757870-G-A

12008889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757870-G-C

12008889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111757870-G-T

12008948-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111757942-G-C

12008948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111757942-G-T

12008960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111757949-G-A

12008960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111757949-G-T

http://identifiers.org/hco/11/GRCh38#12008970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111757959-C-A

12008970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111757959-C-G

12008993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758001-G-T

http://identifiers.org/hco/11/GRCh38#12009003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758011-C-A

12009003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758011-C-T

12009015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758023-C-T

12009044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758052-G-A

12009044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758052-G-T

12009063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758078-G-A

12009063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758078-G-C

12009063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758078-G-T

12009091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 111758096-T-G

http://identifiers.org/hco/11/GRCh38#12009155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758160-C-A

http://identifiers.org/hco/11/GRCh38#12009171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758176-C-A

12009171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 111758176-C-T

http://identifiers.org/hco/11/GRCh38#12009215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758215-C-A

12009215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758215-C-T

12009230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758223-G-A

12009255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758247-G-A

12009269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758261-G-T

12009301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758273-T-C

12009320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758291-G-A

12009320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 111758291-G-T

12009378-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758338-C-G

12009378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758338-C-T

12009451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758378-G-A

12009451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758378-G-T

12009454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758381-G-A

12009454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758381-G-T

http://identifiers.org/hco/11/GRCh38#12009518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758433-C-A

12009518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758433-C-T

http://identifiers.org/hco/11/GRCh38#12009569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/7/GRCm39#111758482-C-A

12009569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758482-C-G

12009569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 111758482-C-T

12009730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2893
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 111758593-G-A