236214972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624909-G-T

236215115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624788-T-C

236215230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624679-C-G

http://identifiers.org/hco/1/GRCh38#236215338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12624595-C-A

236215412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624560-C-T

236215419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624553-A-G

236215438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624528-G-C

236215438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624528-G-T

236215491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624476-A-G

http://identifiers.org/hco/1/GRCh38#236215521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12624454-C-A

236215521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624454-C-T

236215533-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624437-G-C

236215533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624437-G-T

236215648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624321-T-C

236215652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624317-G-A

236215652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624317-G-T

236215660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624309-T-C

236215701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624269-C-T

236215719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624251-A-G

236215719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624251-A-T

236215753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624217-C-T

236215857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624149-T-C

http://identifiers.org/hco/1/GRCh38#236215905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12624100-C-A

236215928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624072-A-T

http://identifiers.org/hco/1/GRCh38#236215995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12624048-C-A

236216044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12624005-C-T

http://identifiers.org/hco/1/GRCh38#236216109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12623956-C-A

236216119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623946-A-T

236216337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623750-A-G

236216344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623743-A-G

236216407-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623664-A-T

236216614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623504-C-T

236216805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623311-T-G

236216825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623292-A-G

http://identifiers.org/hco/1/GRCh38#236216869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12623248-C-A

236216869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623248-C-T

http://identifiers.org/hco/1/GRCh38#236216870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12623247-C-A

236216870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623247-C-T

236216954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623153-C-T

http://identifiers.org/hco/1/GRCh38#236217035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12623077-C-A

236217057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623055-G-A

236217074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12623041-G-T

236217178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622944-T-C

236217266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622871-T-C

236217418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622729-A-G

236217458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622693-G-T

http://identifiers.org/hco/1/GRCh38#236217551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12622613-A-C

http://identifiers.org/hco/1/GRCh38#236217800-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12622386-A-C

http://identifiers.org/hco/1/GRCh38#236217835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12622360-C-A

236218038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622199-T-G

http://identifiers.org/hco/1/GRCh38#236218081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12622159-C-A

236218081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622159-C-T

236218087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622153-T-C

236218147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622093-T-A

236218147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622093-T-C

236218212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12622032-A-G

236218432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12621856-T-C

236218478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12621809-T-C

236218490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12621798-T-A

236218490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12621798-T-C

http://identifiers.org/hco/1/GRCh38#236218574-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12621716-A-C

236218574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12621716-A-G

236218574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12621716-A-T

236218581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12621708-G-A

236218581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12621708-G-T

236218628-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621656-T-A

236218628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621656-T-C

http://identifiers.org/hco/1/GRCh38#236218642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12621642-A-C

236218642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621642-A-G

236218642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621642-A-T

236218681-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621598-T-A

236218681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621598-T-C

236218681-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621598-T-G

http://identifiers.org/hco/1/GRCh38#236218689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12621588-C-A

236218689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621588-C-T

236218721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621549-T-C

http://identifiers.org/hco/1/GRCh38#236218728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12621542-A-C

236218772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621466-A-G

236218960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621268-C-T

236218962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621266-C-T

236219016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621214-T-C

236219134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621030-T-C

236219150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12621012-G-A

236219302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12620672-C-T

236219568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12620438-A-G

236219682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12620323-G-A

http://identifiers.org/hco/1/GRCh38#236220112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12619927-C-A

236220144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12619901-T-C

236220182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619847-C-T

236220341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619710-T-A

236220584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619577-A-T

236220589-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619572-T-A

236220589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619572-T-C

236220589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619572-T-G

http://identifiers.org/hco/1/GRCh38#236220614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12619558-C-A

236220614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619558-C-T

236220681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619481-A-G

236220681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619481-A-T

http://identifiers.org/hco/1/GRCh38#236220687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12619475-A-C

236220687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619475-A-T

236220715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619453-A-G

236220715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619453-A-T

236220739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619429-A-G

236220775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619389-G-T

236220889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619291-G-C

236220908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619272-G-A

236220911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619269-T-C

236220934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12619246-A-G

http://identifiers.org/hco/1/GRCh38#236220973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12619207-A-C

236220973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12619207-A-G

http://identifiers.org/hco/1/GRCh38#236221869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12617340-C-A

236221869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12617340-C-T

236221885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12617324-G-T

236221915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617293-C-T

http://identifiers.org/hco/1/GRCh38#236221976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12617232-C-A

236221976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12617232-C-T

236222061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617153-G-A

236222061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617153-G-C

236222061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12617153-G-T

http://identifiers.org/hco/1/GRCh38#236225084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12616678-C-A

236225084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616678-C-T

236225128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616634-A-G

236225128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12616634-A-T

http://identifiers.org/hco/1/GRCh38#236225210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12616563-A-C

236225210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616563-A-G

236225216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616557-T-C

236225223-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616550-T-A

236225223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616550-T-C

236225223-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616550-T-G

236225431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12616019-A-G

236225461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615985-C-T

236225543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615907-G-A

http://identifiers.org/hco/1/GRCh38#236225560-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12615892-A-C

236226007-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615454-T-G

236226068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615383-T-C

http://identifiers.org/hco/1/GRCh38#236226127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12615336-C-A

236226136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615327-T-C

236226136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615327-T-G

236226162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615317-A-T

236226216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615269-C-T

236226224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615261-G-T

236226247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12615242-A-G

236226290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12615199-A-G

236226322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 12615167-T-G

236226323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12615166-G-C

236226386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12615103-C-T

236226468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12615021-G-A

236226503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614986-T-C

236226503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614986-T-G

236226535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12614954-C-T

236226538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12614951-T-C

236226540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12614949-C-T

236226639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12614848-A-G

236226819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614671-G-T

http://identifiers.org/hco/1/GRCh38#236226867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12614403-A-C

236226867-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614403-A-T

236226870-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614400-T-A

236226940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614239-T-C

236226977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614202-G-A

236227084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614096-T-A

236227115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12614062-C-T

236227196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12613953-C-T

236227228-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12613921-G-C

236227423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12613745-T-A

236227423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12613745-T-C

236227624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612936-C-G

236227728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612841-A-G

236227802-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612773-A-G

236227825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612750-C-T

236228033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612580-A-G

236228261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612259-A-G

236228335-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612195-T-A

http://identifiers.org/hco/1/GRCh38#236228336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12612192-A-C

236228336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612192-A-G

236228351-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612177-T-G

236228426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12612108-C-T

236228604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611956-T-C

236228668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611859-A-G

236228711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611818-T-C

236228713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611816-T-C

236228883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611667-G-A

236228883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611667-G-C

236229510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611184-T-C

236229733-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12611000-T-G

236229906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12610847-T-C

236229939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12610814-G-C

http://identifiers.org/hco/1/GRCh38#236230098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12610670-C-A

236230098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12610670-C-T

236230201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12610619-T-A

236230201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12610619-T-C

http://identifiers.org/hco/1/GRCh38#236230655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12610498-A-C

236230769-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610388-T-A

236230798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610362-T-A

http://identifiers.org/hco/1/GRCh38#236230985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12610310-C-A

236230987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610308-T-C

236230989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610306-G-A

236231018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610287-C-T

http://identifiers.org/hco/1/GRCh38#236231029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12610276-A-C

236231325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12610052-A-G

236231419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609960-C-T

236232040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609453-G-A

http://identifiers.org/hco/1/GRCh38#236232100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12609396-C-A

236232272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609242-C-T

236232332-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12609188-G-C

http://identifiers.org/hco/1/GRCh38#236232349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12609174-A-C

http://identifiers.org/hco/1/GRCh38#236232589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12608633-C-A

236232589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608633-C-G

236233078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608171-G-A

236233100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608156-A-T

236233193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12608104-C-T

236233813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607782-G-A

236233919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607725-C-T

236233945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607699-A-G

236234367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607308-C-G

236234381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607297-T-C

236234426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607251-G-A

236234661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12607041-C-T

236234961-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606776-G-C

236235026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606717-A-G

http://identifiers.org/hco/1/GRCh38#236235110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12606606-A-C

236235165-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606562-A-T

236235222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12606497-G-A

236235839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12605860-A-T

236235854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605847-T-C

http://identifiers.org/hco/1/GRCh38#236235856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12605845-C-A

236235856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605845-C-T

236235880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605821-T-A

236235880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605821-T-C

236235904-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605801-T-A

236235904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605801-T-C

http://identifiers.org/hco/1/GRCh38#236236260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12605781-C-A

236236260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12605781-C-T

236236342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12605696-T-C

236236342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12605696-T-G

236236458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605614-A-G

236236536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12605550-T-C

http://identifiers.org/hco/1/GRCh38#236236576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12605512-A-C

236238688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603879-T-A

236239139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12603418-T-C

236239315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603298-C-T

236239389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603235-C-T

236239484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12603155-A-G

http://identifiers.org/hco/1/GRCh38#236240321-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12602800-A-C

236240514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602611-A-G

http://identifiers.org/hco/1/GRCh38#236240518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12602607-A-C

236240520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602605-C-G

236240626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602522-A-G

236240742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12602424-G-A

http://identifiers.org/hco/1/GRCh38#236241044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12602187-A-C

236242197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12600288-T-C

236242647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599228-T-A

236242809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599061-T-A

236242809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12599061-T-C

236242851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12599025-T-C

236242920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598957-G-A

236242922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598955-C-T

236242939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598938-C-T

236242959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598916-A-T

236242962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598913-T-A

236242962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598913-T-C

236243258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598646-G-A

236243293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598611-T-C

236243294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598610-G-A

236243294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598610-G-T

236243333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598573-T-C

236243334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598572-A-G

236243334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598572-A-T

236243350-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598556-T-G

236243376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598530-A-G

236243376-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598530-A-T

236243412-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598499-A-T

236243445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12598466-C-G

236243445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12598466-C-T

236243519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598400-G-T

236243521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598398-A-G

236243556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598364-T-C

236243580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598339-A-G

236243606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598323-A-G

236243676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12598262-G-A

236249391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597208-T-G

236249486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597106-G-A

236249486-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12597106-G-C

236249596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596999-T-C

236249635-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596981-G-C

http://identifiers.org/hco/1/GRCh38#236249789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596864-C-A

236249805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596845-A-G

http://identifiers.org/hco/1/GRCh38#236249821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596829-C-A

236249821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596829-C-G

236249821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596829-C-T

http://identifiers.org/hco/1/GRCh38#236249842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596782-A-C

236249856-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596693-T-A

236249894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12596621-C-T

236249942-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12596573-T-G

236250009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596504-T-C

http://identifiers.org/hco/1/GRCh38#236250032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596496-C-A

236250032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596496-C-T

http://identifiers.org/hco/1/GRCh38#236250050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596491-A-C

236250050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596491-A-G

http://identifiers.org/hco/1/GRCh38#236250092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596466-A-C

236250092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596466-A-G

236250923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12596182-T-C

http://identifiers.org/hco/1/GRCh38#236251020-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596092-A-C

http://identifiers.org/hco/1/GRCh38#236251149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12596023-C-A

236251191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595987-T-C

236251405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595821-A-G

236251413-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595813-T-C

236251424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 12595809-A-G

236251473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12595784-G-A

236251475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12595782-G-C

236251544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12595722-T-C

http://identifiers.org/hco/1/GRCh38#236251557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12595712-C-A

236251582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12595688-G-A

236251582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12595688-G-T

http://identifiers.org/hco/1/GRCh38#236251689-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12595598-A-C

236251689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595598-A-T

236251813-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595502-G-C

236251832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595483-C-G

236251832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595483-C-T

236251899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595417-G-A

236251899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595417-G-T

236251940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595377-T-C

236251984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595328-G-A

236251984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595328-G-T

236251985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595327-T-A

236252018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595326-G-A

236252018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595326-G-T

236252023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595321-A-G

236252037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595307-A-G

236252037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12595307-A-T

236253114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594399-T-G

236253120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594393-A-G

236253168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594359-T-C

http://identifiers.org/hco/1/GRCh38#236253243-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12594286-C-A

http://identifiers.org/hco/1/GRCh38#236253331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12594222-C-A

236253331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594222-C-T

236253355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594209-T-C

236253365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594199-G-A

236253365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594199-G-T

236253391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594173-T-C

236253391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594173-T-G

236253549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594006-G-T

236253551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594004-G-A

236253551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12594004-G-T

236253582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593975-C-T

236253591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593966-G-A

236253591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593966-G-T

236253634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593922-T-A

236253637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593919-G-A

236253637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593919-G-T

http://identifiers.org/hco/1/GRCh38#236253649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12593907-A-C

236253649-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593907-A-T

236253968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593539-G-T

236254231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12593306-T-C

236266918-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591806-T-A

236266918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591806-T-C

236266947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591793-T-C

236267235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591430-T-C

236267349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591320-A-G

236267424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591247-A-T

236267608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591069-G-A

http://identifiers.org/hco/1/GRCh38#236267635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12591042-C-A

236267635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12591042-C-T

236268070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12590856-T-C

236268098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12590830-T-C

236269439-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12590200-A-T

236269638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12590026-C-T

236269724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589937-G-A

236269724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589937-G-T

236269731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589935-A-T

236269749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589917-A-G

236269749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589917-A-T

236269802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589875-G-A

236269802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589875-G-C

236269802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589875-G-T

http://identifiers.org/hco/1/GRCh38#236269827-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12589864-C-A

236269827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12589864-C-T

http://identifiers.org/hco/1/GRCh38#236269966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12589727-C-A

236269968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 12589725-C-T

236269998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12589695-G-A

236269998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12589695-G-C

236269998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12589695-G-T

236269999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 12589694-A-G

236270011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589674-T-C

236270021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589664-T-C

236270032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589653-T-C

236270036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589649-T-C

236270067-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589623-A-T

236270095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589595-G-A

236270095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589595-G-T

236270138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589347-T-C

236270145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589340-T-C

236270378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12589127-T-G

236270909-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588424-A-G

236271027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12588189-A-G

236271243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587926-G-T

236271341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587840-G-T

236271387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587792-T-C

236271450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12587746-G-A

236278347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583545-T-C

236278468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583484-G-A

236278468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583484-G-C

236278501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583449-C-G

236278505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583440-T-G

http://identifiers.org/hco/1/GRCh38#236278544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12583402-C-A

http://identifiers.org/hco/1/GRCh38#236278670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12583293-C-A

236278670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583293-C-T

236278683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12583280-C-T

236279152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582835-T-A

236279152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582835-T-C

236279202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12582766-A-G

236280679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581913-A-G

236280823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581761-G-T

236280852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581732-C-T

236280876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581708-A-T

236280886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581698-A-G

236281018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581563-G-C

236281244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581366-G-A

236281331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581312-C-T

236281371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581287-T-C

236281474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581205-G-A

236281474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581205-G-T

236281521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581161-T-C

236281526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581156-G-A

236281526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581156-G-T

http://identifiers.org/hco/1/GRCh38#236281530-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12581152-A-C

236281530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581152-A-G

236281589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581120-T-C

236281589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 12581120-T-G

236281604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581103-G-A

236281604-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581103-G-C

236281604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581103-G-T

236281612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581095-G-A

236281612-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581095-G-C

236281612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 12581095-G-T

236281675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 12581064-G-T

236281683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 12581056-T-A

236281683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 12581056-T-C

236281683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant, undefined
orthologous variants: 12581056-T-G

236281692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 12581047-A-G

236281731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12581008-A-G

236281731-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12581008-A-T

http://identifiers.org/hco/1/GRCh38#236281772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12580967-C-A

236281772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 12580967-C-T

http://identifiers.org/hco/1/GRCh38#236281773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12580966-C-A

236281773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580966-C-T

http://identifiers.org/hco/1/GRCh38#236281834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#12580908-C-A

236281834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580908-C-G

236281834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580908-C-T

236281863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580879-G-A

236281863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580879-G-T

236281883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580859-G-A

236281883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580859-G-C

236281883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 12580859-G-T

236281933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580810-T-C

236281933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580810-T-G

236281934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580809-T-A

236281934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580809-T-C

236281934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580809-T-G

236281953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580792-G-A

http://identifiers.org/hco/1/GRCh38#236281954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#12580791-C-A

236281954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14355
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 12580791-C-T