115841647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 46874705-A-G

115841884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46874929-G-A

115841884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46874929-G-C

115841884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 46874929-G-T

115841964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46875004-A-G

115842214-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875245-T-A

115842259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875281-G-T

115842285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875308-T-G

http://identifiers.org/hco/5/GRCh38#115842389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46875379-C-A

115842389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875379-C-T

115842398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875388-G-A

115842398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875388-G-T

http://identifiers.org/hco/5/GRCh38#115842545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46875476-C-A

115842545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46875476-C-T

http://identifiers.org/hco/5/GRCh38#115842575-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46875501-A-C

115842575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 46875501-A-G

115842587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875513-T-A

115842840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875761-G-T

115843053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46875965-G-A

115843163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46876063-G-C

115843273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46876175-A-G

115843273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46876175-A-T

http://identifiers.org/hco/5/GRCh38#115843577-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46876489-A-C

115843712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46876597-A-G

115843770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46876750-T-C

115843971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877045-C-T

115844021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877085-G-A

http://identifiers.org/hco/5/GRCh38#115844161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46877224-C-A

http://identifiers.org/hco/5/GRCh38#115844316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46877363-A-C

115844344-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877394-G-A

115844409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877452-T-C

115844455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877497-G-T

115844687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877714-G-C

115844858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46877868-C-T

115845105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46878492-C-T

115845270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46878845-G-A

115845270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46878845-G-T

http://identifiers.org/hco/5/GRCh38#115866234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46886999-A-C

115866234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46886999-A-G

115866498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46887268-C-T

115866520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46887290-C-T

115866826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46887590-A-G

115867199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46887931-G-A

115867208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46887943-C-T

115868323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46889825-T-G

115868393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46889897-C-G

115868395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46889899-C-T

115868552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890053-A-G

http://identifiers.org/hco/5/GRCh38#115869000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46890103-C-A

115869000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890103-C-T

115869051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890151-A-G

115869139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890237-G-A

115869177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890277-T-C

115869439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890545-T-G

115869559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890660-G-T

115869609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890680-T-C

115869632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890703-T-C

115869632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890703-T-G

115869779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890836-G-A

115869779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46890836-G-T

115870179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891230-A-G

115870194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891244-T-C

115870194-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891244-T-G

115870198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891248-T-C

http://identifiers.org/hco/5/GRCh38#115870403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46891756-C-A

115870403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891756-C-G

115870472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891812-G-T

115870473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891813-G-A

115870473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46891813-G-T

115871007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892300-G-A

115871007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892300-G-C

115871064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892352-G-A

115871107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892389-C-G

115871169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892446-G-A

http://identifiers.org/hco/5/GRCh38#115871235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46892512-C-A

115871235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892512-C-T

115871324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892591-G-A

115871574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892867-A-G

115871576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46892869-T-C

http://identifiers.org/hco/5/GRCh38#115871585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46892878-A-C

115872367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46901889-T-G

115872465-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46901988-T-A

115872620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902148-G-T

115872755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902278-A-G

115873017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902515-G-A

115873017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902515-G-T

115873125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902604-T-G

115873246-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46902703-T-C

115874104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46903845-G-A

115874180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904017-G-T

115874357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904190-T-C

115874447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904277-A-G

115874467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904292-C-T

http://identifiers.org/hco/5/GRCh38#115874970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46904732-A-C

115874996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904747-C-T

115875119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904848-G-A

115875128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46904857-C-G

http://identifiers.org/hco/5/GRCh38#115875256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46905170-A-C

115875285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905199-C-T

115875346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905260-C-T

http://identifiers.org/hco/5/GRCh38#115875357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46905271-C-A

115875419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905333-C-G

115875419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905333-C-T

115875507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905412-C-T

115875606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905510-A-G

http://identifiers.org/hco/5/GRCh38#115875633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46905536-C-A

115875761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905653-C-G

115875802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905738-G-A

115875826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46905787-G-C

http://identifiers.org/hco/5/GRCh38#115875859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46905811-C-A

115888289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46909663-G-T

115888369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46909725-G-A

115888369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46909725-G-T

115888704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46910464-G-A

115888730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46910490-T-C

115888797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46910562-A-G

115888856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46910625-C-T

115889145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46910918-A-G

115889297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911069-T-C

115889304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911076-A-T

115889384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911156-C-T

115889615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911327-C-T

115894580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911805-A-G

115894584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911809-T-C

115894607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911820-A-T

115894630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46911844-G-T

115894905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912097-G-C

115894985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912150-A-G

http://identifiers.org/hco/5/GRCh38#115895196-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46912375-A-C

http://identifiers.org/hco/5/GRCh38#115895288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46912450-C-A

115895288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912450-C-T

115895311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912474-G-A

115895311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912474-G-T

115895314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912477-G-C

115895346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912513-A-T

115895392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912534-A-G

115895533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912673-G-A

115895590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912728-C-T

115895673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46912811-G-A

115902707-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46913585-T-A

115902707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46913585-T-C

http://identifiers.org/hco/5/GRCh38#115902780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46913652-C-A

115902780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46913652-C-T

115902847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46913699-A-T

115903023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913867-G-A

115903023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913867-G-T

115903038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913882-A-G

115903058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913909-A-G

115903064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913915-C-G

http://identifiers.org/hco/5/GRCh38#115903074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46913925-C-A

115903074-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913925-C-G

115903074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913925-C-T

115903107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913955-G-A

115903107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913955-G-T

http://identifiers.org/hco/5/GRCh38#115903108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46913956-C-A

115903108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913956-C-T

115903127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46913975-A-G

115903176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914026-A-T

115903426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914134-G-A

115903426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914134-G-T

115903578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914260-A-G

115903646-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914315-T-G

115903680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914348-G-A

115903777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914425-G-A

115903777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914425-G-T

115904053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914606-G-A

115904053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 46914606-G-T

http://identifiers.org/hco/5/GRCh38#115904275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46914795-A-C

http://identifiers.org/hco/5/GRCh38#115904938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46915414-A-C

115905128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46915556-T-C

115905161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46915564-A-G

115905397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46915794-C-T

http://identifiers.org/hco/5/GRCh38#115906526-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46916547-A-C

115906575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916600-T-C

115906594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916619-G-A

115906594-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916619-G-C

http://identifiers.org/hco/5/GRCh38#115906621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46916645-C-A

115906666-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916678-T-G

115906699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916710-T-C

115906731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46916739-T-C

http://identifiers.org/hco/5/GRCh38#115907141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46917156-C-A

115907246-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917256-A-T

115907482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917519-C-T

115907530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917543-A-G

115907577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917567-C-T

115907832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917805-T-C

115907943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917957-A-G

115907969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917977-T-G

115907981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46917989-C-T

115908062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

http://identifiers.org/hco/5/GRCh38#115908484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46918410-A-C

115908560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46918486-T-C

115908584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46918510-A-G

115908766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46918934-T-C

115909029-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46919340-A-T

115909314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46919609-C-T

115909578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46919874-A-G

115909694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46919987-A-G

115910410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920060-G-C

115910417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920067-T-C

115910968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920582-A-G

115911136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920747-G-A

115911383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920932-A-T

115911457-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46920992-C-G

115911762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921402-T-A

115911799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921441-G-A

115911885-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921524-T-A

115911960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921599-T-C

115911964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921603-A-G

115912230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46921866-G-T

115912570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922200-T-G

http://identifiers.org/hco/5/GRCh38#115912651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46922263-C-A

115912735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922340-A-T

115912891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922499-C-G

115913122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922723-G-A

http://identifiers.org/hco/5/GRCh38#115913227-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46922830-C-A

115913227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922830-C-T

http://identifiers.org/hco/5/GRCh38#115913255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46922856-C-A

115913255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922856-C-G

115913255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 46922856-C-T

115913532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923132-A-G

115913577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923177-G-A

115913577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923177-G-T

http://identifiers.org/hco/5/GRCh38#115913586-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46923186-A-C

115913586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923186-A-G

115913602-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923201-T-A

http://identifiers.org/hco/5/GRCh38#115913668-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46923267-C-A

115913668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923267-C-G

115913668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923267-C-T

115913696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923295-T-C

115913711-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923324-T-G

115913712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923325-T-C

http://identifiers.org/hco/5/GRCh38#115913760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/18/GRCm39#46923374-A-C

115913760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923374-A-G

115913783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923397-T-A

115913798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923408-A-G

115913849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923459-C-G

115913849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923459-C-T

115914032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2013
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 46923637-C-T