74326304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 114656294-A-G

74326338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 114656328-C-T

http://identifiers.org/hco/17/GRCh38#74326478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114656444-C-A

74326478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656444-C-T

74326613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656556-A-G

74326791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656692-C-T

74327022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656934-G-A

74327042-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656952-C-G

74327074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656974-C-T

74327099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114656998-G-A

74327713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657365-C-T

74328091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657624-C-G

74328170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657704-G-C

74328297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657839-G-T

74328373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657937-G-A

74328406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657964-G-A

74328406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114657964-G-T

74328669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658164-G-A

74328669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658164-G-T

74328735-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658230-G-C

74328743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658238-T-C

74328790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658286-G-T

74328800-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658296-C-G

74328878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658370-T-C

74328881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658373-G-A

74328881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658373-G-T

http://identifiers.org/hco/17/GRCh38#74328882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114658374-C-A

74328882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658374-C-T

74328947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658435-A-G

74328947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114658435-A-T

http://identifiers.org/hco/17/GRCh38#74328999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114658487-C-A

74329298-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114659380-T-A

74329298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114659380-T-C

74329467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114659481-G-A

74329467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114659481-G-C

http://identifiers.org/hco/17/GRCh38#74329488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114659502-C-A

74329491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114659505-G-T

74329571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114659591-G-A

74329595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114659611-G-T

74329930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114660014-C-T

74330881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114661112-A-G

74331326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114661816-G-A

74331326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114661816-G-C

74331370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114661901-G-A

http://identifiers.org/hco/17/GRCh38#74331417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114661950-C-A

74331498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662028-G-T

74331508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662038-C-T

74331616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662151-A-G

74331639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662181-C-T

74331938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662456-G-A

74332078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662576-A-G

74332181-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662676-T-A

74332264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662720-A-G

74332446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662840-G-T

74332515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662888-G-A

74332554-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114662929-A-G

74332918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114663165-C-T

74333031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 114663250-A-T

http://identifiers.org/hco/17/GRCh38#74333271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114663432-A-C

74334190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114663670-A-G

http://identifiers.org/hco/17/GRCh38#74334200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114663680-C-A

74334200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114663680-C-T

74334221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114663700-G-A

74334393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114663874-C-G

74334436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114663919-A-G

74334681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664132-C-T

74334933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664325-T-C

74335051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664414-C-T

74335072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664435-C-T

74335151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664497-C-T

74335190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664537-G-A

74335204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664551-G-T

http://identifiers.org/hco/17/GRCh38#74335244-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114664583-C-A

http://identifiers.org/hco/17/GRCh38#74335449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114664782-C-A

74335449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664782-C-G

74335495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664826-C-G

74335495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664826-C-T

74335601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664911-C-T

74335627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114664936-G-T

74337687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114665790-A-G

74337753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114665849-T-C

74337983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666086-G-T

74338259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666325-G-C

74338342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666395-G-A

74338477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666614-C-G

74338477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666614-C-T

74338669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666742-A-G

74338812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666869-G-A

74338901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114666958-C-T

74339232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114667276-G-A

74339232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114667276-G-T

http://identifiers.org/hco/17/GRCh38#74339241-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114667284-A-C

74339621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114667701-G-A

74340153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668112-A-G

74340162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668121-C-T

74340191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668153-G-A

74340267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668219-T-C

74340433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114668347-G-C

74340435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114668349-G-A

74340522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114668410-T-G

74340548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668426-C-T

74340551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668429-G-A

http://identifiers.org/hco/17/GRCh38#74340606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114668482-C-A

74340606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668482-C-T

74340631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114668512-G-A

74341827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669129-G-T

http://identifiers.org/hco/17/GRCh38#74341859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669161-C-A

74341859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669161-C-G

74341896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114669200-A-G

74341896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114669200-A-T

http://identifiers.org/hco/17/GRCh38#74341911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669215-C-A

74341911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114669215-C-G

74341911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114669215-C-T

74341992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669296-G-A

74341992-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669296-G-C

74342038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669374-G-T

74342042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669378-C-T

74342062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669396-G-T

74342063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669397-G-C

http://identifiers.org/hco/17/GRCh38#74342071-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669410-C-A

74342071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669410-C-T

http://identifiers.org/hco/17/GRCh38#74342072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669411-C-A

74342101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669432-T-A

74342101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669432-T-C

http://identifiers.org/hco/17/GRCh38#74342125-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669454-C-A

74342125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669454-C-T

http://identifiers.org/hco/17/GRCh38#74342127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669456-C-A

74342127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669456-C-G

74342127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669456-C-T

http://identifiers.org/hco/17/GRCh38#74342128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669457-A-C

74342128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669457-A-G

74342128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669457-A-T

74342138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669494-G-T

74342149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669505-C-T

74342162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669552-C-T

74342215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669608-A-G

74342227-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669632-G-A

74342240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669657-T-C

http://identifiers.org/hco/17/GRCh38#74342394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669812-C-A

74342394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669812-C-G

74342394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669812-C-T

74342419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669841-G-A

74342453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669876-G-A

http://identifiers.org/hco/17/GRCh38#74342492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114669914-C-A

74342492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669914-C-G

74342492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669914-C-T

74342524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669946-G-A

74342524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669946-G-T

74342536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669958-G-C

74342536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114669958-G-T

http://identifiers.org/hco/17/GRCh38#74342710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670118-C-A

74342710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114670118-C-T

74342734-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670142-G-C

74342735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670143-A-G

http://identifiers.org/hco/17/GRCh38#74342788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670211-C-A

http://identifiers.org/hco/17/GRCh38#74342895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670293-C-A

74342895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670293-C-T

74342942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670329-A-G

http://identifiers.org/hco/17/GRCh38#74343100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670487-C-A

http://identifiers.org/hco/17/GRCh38#74343215-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670614-C-A

74343215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670614-C-T

74343221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670619-G-A

http://identifiers.org/hco/17/GRCh38#74343252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670649-C-A

74343252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114670649-C-T

http://identifiers.org/hco/17/GRCh38#74343380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114670799-A-C

74343779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671220-C-T

74343987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671375-G-T

74344164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671527-G-A

74344164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671527-G-T

74344303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114671659-C-T

74344321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114671677-C-T

74344367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671723-G-A

74344371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671727-G-A

74344376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671732-C-G

74344376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671732-C-T

http://identifiers.org/hco/17/GRCh38#74344391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114671747-C-A

74344391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671747-C-T

74344457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671793-G-A

http://identifiers.org/hco/17/GRCh38#74344644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114671921-C-A

74344644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114671921-C-T

74344859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114672095-C-G

74344859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114672095-C-T

74344964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672200-G-T

http://identifiers.org/hco/17/GRCh38#74345033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114672289-A-C

74345033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672289-A-G

74345033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672289-A-T

http://identifiers.org/hco/17/GRCh38#74346240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114672530-C-A

74346252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672539-A-G

74346306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672580-G-T

74346311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672585-G-A

74346311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672585-G-T

http://identifiers.org/hco/17/GRCh38#74346533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114672785-C-A

74346533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 114672785-C-T

74346540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 114672792-G-A

74346641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672870-A-G

http://identifiers.org/hco/17/GRCh38#74346655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114672883-A-C

74346655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672883-A-G

74346658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672886-T-A

74346658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672886-T-G

74346719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114672944-A-G

74346803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673037-C-T

74347029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673264-G-T

http://identifiers.org/hco/17/GRCh38#74347190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673405-C-A

http://identifiers.org/hco/17/GRCh38#74347708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673736-C-A

74347708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673736-C-T

http://identifiers.org/hco/17/GRCh38#74347714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673742-C-A

74347714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673742-C-T

http://identifiers.org/hco/17/GRCh38#74347763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673791-C-A

74347763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673791-C-T

http://identifiers.org/hco/17/GRCh38#74347766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673794-C-A

74347766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673794-C-T

http://identifiers.org/hco/17/GRCh38#74347872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114673900-C-A

74347872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114673900-C-G

74347872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114673900-C-T

74347902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673930-G-A

74347902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673930-G-C

74347902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114673930-G-T

http://identifiers.org/hco/17/GRCh38#74347978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114674004-C-A

74347978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674004-C-T

74348132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674145-T-C

74348264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674270-G-T

http://identifiers.org/hco/17/GRCh38#74348312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114674313-C-A

74348312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674313-C-T

74348320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674321-A-G

74348506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674473-G-A

74348506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114674473-G-T

http://identifiers.org/hco/17/GRCh38#74348599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114674613-A-C

http://identifiers.org/hco/17/GRCh38#74348606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114674640-C-A

74348606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114674640-C-T

http://identifiers.org/hco/17/GRCh38#74348669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114674736-C-A

74348669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114674736-C-G

74348709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114674784-G-A

74348709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114674784-G-T

74348745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114674825-G-T

74348916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675082-A-G

74348963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675134-G-A

74348963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675134-G-T

http://identifiers.org/hco/17/GRCh38#74348972-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675143-A-C

74348972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675143-A-G

74348972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675143-A-T

74348979-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675144-T-A

74348979-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675144-T-G

http://identifiers.org/hco/17/GRCh38#74348983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675148-C-A

74348983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675148-C-T

http://identifiers.org/hco/17/GRCh38#74349000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675165-C-A

74349000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675165-C-T

74349014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675194-G-A

74349014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675194-G-T

74349088-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675275-T-A

74349161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 114675553-C-T

74349240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114675633-C-T

http://identifiers.org/hco/17/GRCh38#74349315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675708-C-A

74349381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114675793-C-T

http://identifiers.org/hco/17/GRCh38#74349412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675824-C-A

74349412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114675824-C-T

http://identifiers.org/hco/17/GRCh38#74349493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114675876-C-A

74350320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114676197-G-A

74350366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114676229-C-T

74350435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114676295-G-C

74350435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 114676295-G-T

http://identifiers.org/hco/17/GRCh38#74350581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114676445-C-A

74350581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114676445-C-G

74350581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 114676445-C-T

http://identifiers.org/hco/17/GRCh38#74350728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114676582-C-A

74350746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114676600-G-A

74350866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 114676717-A-G

http://identifiers.org/hco/17/GRCh38#74350948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114676789-C-A

74350948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676789-C-T

74351063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676872-T-A

74351126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676935-G-A

74351126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676935-G-T

74351130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676939-G-A

74351130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676939-G-T

74351153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 114676962-A-G

74351746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677107-G-A

74351746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677107-G-T

74351752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677113-G-A

74351752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677113-G-T

http://identifiers.org/hco/17/GRCh38#74351760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677121-C-A

74351760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677121-C-T

http://identifiers.org/hco/17/GRCh38#74351812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677158-C-A

74351812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677158-C-T

http://identifiers.org/hco/17/GRCh38#74351912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677247-C-A

74351912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 114677247-C-T

http://identifiers.org/hco/17/GRCh38#74351941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677276-C-A

74351941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 114677276-C-T

http://identifiers.org/hco/17/GRCh38#74352025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677360-C-A

74352025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 114677360-C-T

74352046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 114677381-G-A

74352046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 114677381-G-T

74352067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 114677402-C-G

74352067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 114677402-C-T

74352115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, missense_variant
orthologous variants: 114677450-G-T

74352141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677476-G-T

http://identifiers.org/hco/17/GRCh38#74352144-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677479-C-A

74352144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 114677479-C-T

74352155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114677488-G-A

74352183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114677516-G-A

74352183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114677516-G-T

http://identifiers.org/hco/17/GRCh38#74352192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114677525-C-A

74352198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677531-G-A

74352210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 114677548-C-G

74352238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 114677577-G-A

74352355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677691-G-T

74352363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114677699-T-C

74352699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678205-G-A

74352699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678205-G-T

http://identifiers.org/hco/17/GRCh38#74352714-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114678216-C-A

74352714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678216-C-G

74352714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678216-C-T

http://identifiers.org/hco/17/GRCh38#74352764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114678249-C-A

74352764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678249-C-T

74353066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678509-G-A

74353066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678509-G-T

74353085-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114678528-A-T

http://identifiers.org/hco/17/GRCh38#74353096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114678539-C-A

http://identifiers.org/hco/17/GRCh38#74353419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114678826-C-A

74353508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114678914-C-T

74353541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: 114678947-C-G

74353541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114678947-C-T

http://identifiers.org/hco/17/GRCh38#74353607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114679014-C-A

74353607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114679014-C-T

74353951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114679771-G-A

74353963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114679784-G-A

http://identifiers.org/hco/17/GRCh38#74354026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114679847-C-A

74354026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114679847-C-G

http://identifiers.org/hco/17/GRCh38#74354083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#114679902-C-A

74354083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114679902-C-T

74354093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114679912-C-T

http://identifiers.org/hco/17/GRCh38#74354094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#114679913-C-A

74354094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114679913-C-G

74354095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron_variant, undefined
orthologous variants: 114679914-A-G

74354228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, undefined
orthologous variants: 114680036-C-T

http://identifiers.org/hco/17/GRCh38#74354324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680132-C-A

74354514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680322-G-A

74354514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: 114680322-G-C

74354514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: 114680322-G-T

http://identifiers.org/hco/17/GRCh38#74354538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680346-C-A

http://identifiers.org/hco/17/GRCh38#74354541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680349-C-A

74354541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680349-C-T

http://identifiers.org/hco/17/GRCh38#74354598-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680407-A-C

74354598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680407-A-G

74354598-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680407-A-T

74354668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680478-G-C

74354725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680526-C-T

74354753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680554-G-A

74354753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680554-G-T

74354754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680555-G-A

74354754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680555-G-C

74354754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680555-G-T

http://identifiers.org/hco/17/GRCh38#74354782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680585-C-A

74354782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 114680585-C-G

74354782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 114680585-C-T

74354817-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: 114680620-T-A

74354823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680626-G-A

74354823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680626-G-C

74354823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680626-G-T

74354841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: missense variant
orthologous variants: 114680644-C-G

74354841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114680644-C-T

74355033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680819-C-T

74355051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680833-G-A

74355051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: 114680833-G-C

http://identifiers.org/hco/17/GRCh38#74355058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680840-C-A

http://identifiers.org/hco/17/GRCh38#74355183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114680958-C-A

74355183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 114680958-C-T

74355259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: synonymous variant
orthologous variants: 114681034-C-T

http://identifiers.org/hco/17/GRCh38#74355424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681188-C-A

74355424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681188-C-G

74355424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681188-C-T

http://identifiers.org/hco/17/GRCh38#74355429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681193-C-A

74355429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681193-C-G

74355429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681193-C-T

74355456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681219-C-T

http://identifiers.org/hco/17/GRCh38#74355463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681229-C-A

74355463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681229-C-T

http://identifiers.org/hco/17/GRCh38#74355679-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681423-C-A

74355679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681423-C-T

http://identifiers.org/hco/17/GRCh38#74355698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681442-C-A

74355698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681442-C-T

http://identifiers.org/hco/17/GRCh38#74355713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#114681456-C-A

74355713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681456-C-G

74355713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681456-C-T

74355788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26735
most severe consequence: 3 prime UTR variant
orthologous variants: 114681524-C-T