169861725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34372240-A-G

169861840-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34372123-T-G

169861881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34372078-T-C

169861960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34372067-G-T

169862040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34371991-A-G

169862086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34371964-C-T

169862629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34371434-T-C

169863250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34370872-A-G

169863369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34370757-A-G

169864039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34370109-C-T

169864077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34370071-C-G

169864077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34370071-C-T

169864367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369809-G-A

169864367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369809-G-T

169864512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369667-G-T

169864548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369625-G-A

169864548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369625-G-T

http://identifiers.org/hco/5/GRCh38#169864569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34369605-C-A

169864847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369310-C-T

169865100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34369089-G-T

169865295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368914-G-A

169865344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368865-C-T

169865471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368754-C-G

169865472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368753-C-T

http://identifiers.org/hco/5/GRCh38#169865787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34368505-A-C

169865787-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368505-A-T

169865874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368419-C-T

169866217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368197-T-C

169866232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368182-T-G

169866413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34368037-T-A

169866535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34367913-G-A

169866598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34367850-T-C

169867737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34367701-G-A

http://identifiers.org/hco/5/GRCh38#169867819-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34367624-C-A

http://identifiers.org/hco/5/GRCh38#169868021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34367397-A-C

169868154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34367187-T-G

169868418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34366931-A-T

169868856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34366797-T-G

169869031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34366654-G-A

169869031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34366654-G-T

169869139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34366529-C-T

http://identifiers.org/hco/5/GRCh38#169869674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34366008-C-A

169869771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34365942-G-A

169869817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34365899-C-T

169870190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34365562-G-C

169870292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34365513-T-C

169870308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34365497-A-G

169870875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34364329-A-T

169870931-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34364274-C-G

169871013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34364189-C-T

http://identifiers.org/hco/5/GRCh38#169871032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34364172-C-A

169871159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34364055-C-T

169871374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363873-T-C

169871481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363822-C-T

169871645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363693-C-G

169871913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363440-G-T

169871917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363436-A-G

169871957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363401-A-G

169872358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34363058-A-G

169872495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34362918-G-T

169872499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34362913-A-G

169872687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34362781-A-G

169873299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34362202-T-C

169873478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34362054-G-C

169873561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34361971-A-G

169874016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34361558-G-T

169874024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34361550-G-A

169874532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34361352-A-G

169874551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34361333-C-G

169875054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360908-C-T

169875085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360875-C-G

169875236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360736-G-A

169875236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360736-G-C

169875315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360693-T-C

http://identifiers.org/hco/5/GRCh38#169875372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34360636-C-A

http://identifiers.org/hco/5/GRCh38#169875463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34360556-C-A

169875463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360556-C-T

169875492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360528-G-A

169875538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360483-T-C

169875556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360461-T-C

169875613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360405-G-A

169875613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360405-G-T

169875895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360081-T-C

169875929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34360048-G-A

169876001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359972-G-T

169876057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359919-C-T

169876377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359710-C-T

http://identifiers.org/hco/5/GRCh38#169876396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34359691-A-C

169876611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359497-G-T

169876630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359468-T-C

169876915-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359185-A-T

169877016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34359140-T-C

169877736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34358211-G-A

169877968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34358007-C-G

169877977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34358002-T-C

169878166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357805-G-A

169878200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357760-G-A

169878256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357664-A-G

169878256-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357664-A-T

169878297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357576-A-G

169878836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34357047-G-T

169879307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34356355-C-T

169879678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34355978-G-T

169879755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34355901-G-A

169880087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34355549-A-G

169880429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34355213-C-G

169880859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354850-A-G

http://identifiers.org/hco/5/GRCh38#169881216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34354521-A-C

169881298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 34354418-T-C

169881298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354418-T-G

169881318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354398-A-G

169881318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354398-A-T

169881324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354393-T-C

http://identifiers.org/hco/5/GRCh38#169881360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34354358-C-A

169881422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354296-C-G

169881493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354227-G-A

169881493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354227-G-C

169881493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354227-G-T

169881529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354195-A-G

169881530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354194-T-C

169881553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354186-G-A

169881553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34354186-G-T

169881847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353933-C-T

169881932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353850-A-G

169882141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353703-G-A

http://identifiers.org/hco/5/GRCh38#169882441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34353400-C-A

169882512-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353343-T-A

169882682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353174-C-T

169882752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353104-G-A

169882763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34353093-A-T

169882949-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352907-T-A

169882949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352907-T-C

169882957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352899-T-A

169882961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352895-G-A

169883212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 34352644-T-C

169883615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352241-A-G

169883615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352241-A-T

http://identifiers.org/hco/5/GRCh38#169883747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34352109-A-C

169883747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 34352109-A-T

169883928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351934-A-G

169883969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351894-G-A

169883969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351894-G-T

169884042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351827-A-G

169884042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351827-A-T

169884063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351806-G-A

169884063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351806-G-T

169884117-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351752-T-A

169884137-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351729-T-A

169884137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351729-T-C

169884137-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351729-T-G

http://identifiers.org/hco/5/GRCh38#169884166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34351701-C-A

169884262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351607-T-A

169884292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351577-G-A

169884304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351565-A-G

169884503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351371-T-C

169884521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351353-C-T

http://identifiers.org/hco/5/GRCh38#169884665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34351210-C-A

169884665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351210-C-T

169884800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351070-A-G

169884844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34351026-A-G

169884955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34350952-T-C

169885463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34350069-G-A

169886268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34348479-G-T

169886296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34348451-T-C

169886516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34348256-G-A

http://identifiers.org/hco/5/GRCh38#169886582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34348193-C-A

169886638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34348135-C-T

169886730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34348046-T-C

http://identifiers.org/hco/5/GRCh38#169886876-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34347921-A-C

169886935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347860-A-G

169886997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347801-A-G

169887062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347737-G-A

169887127-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347672-C-G

169887156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347650-T-C

169887220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347594-A-G

169887257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34347568-A-G

169887843-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34346996-C-G

169887843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34346996-C-T

169887859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34346981-A-G

169888029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34346569-T-C

169888471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34346126-A-G

169888785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34345898-A-T

http://identifiers.org/hco/5/GRCh38#169888806-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34345877-A-C

169889065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34345646-C-T

169892275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34344303-C-T

169892812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343847-A-G

169892851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343817-C-T

http://identifiers.org/hco/5/GRCh38#169892888-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34343782-A-C

169892888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343782-A-G

169892888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343782-A-T

http://identifiers.org/hco/5/GRCh38#169892895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34343775-C-A

169893022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343655-C-G

169893076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343598-G-T

169893236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343412-T-A

169893370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343283-C-G

169893669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34343016-C-T

169893943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34342746-T-C

169894706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34342058-T-G

169894776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34342005-A-T

169894876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34341934-A-G

http://identifiers.org/hco/5/GRCh38#169895005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34341842-C-A

169895064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34340340-G-T

169895241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34340203-A-G

169895241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34340203-A-T

http://identifiers.org/hco/5/GRCh38#169895979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34339520-C-A

169895979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339520-C-T

169895996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339503-G-A

169895996-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339503-G-C

http://identifiers.org/hco/5/GRCh38#169896044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34339455-C-A

169896044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339455-C-T

169896095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339406-T-C

169896182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339333-G-A

169896232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339290-T-G

169896274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339252-T-A

169896343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339178-G-T

169896398-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339130-T-G

169896502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339027-G-A

169896544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34339012-A-G

169896602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338954-C-T

169896809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338821-A-G

169897085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338570-A-G

169897088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338567-A-G

169897500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338457-C-T

http://identifiers.org/hco/5/GRCh38#169897531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34338426-A-C

169897610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338382-C-T

169897621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338371-T-C

169897725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338273-A-G

169897857-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338176-T-G

169897935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34338118-G-A

169898270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34337798-G-C

169898356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34337713-T-C

169898356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34337713-T-G

169898677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34337412-A-T

169899219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336944-A-G

169899256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336913-G-A

169899324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336862-C-T

169899427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336779-A-G

169899675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336514-G-A

169899684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336505-G-A

169899871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336275-T-C

169899929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336217-A-G

169900141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34336037-C-G

169900185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335993-G-T

169900378-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335803-T-G

169900439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335739-T-C

169900486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335692-A-G

169900661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335524-T-G

169900816-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335357-T-A

169900841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335331-G-A

169900841-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335331-G-T

169901053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335188-T-C

169901074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335166-C-T

169901244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34335027-A-G

169901401-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34334868-T-G

169901405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34334864-G-T

169901754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34334352-A-G

169901879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34334255-T-A

169902157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34334039-G-A

169902305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333900-G-A

169902413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333836-C-G

169902413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333836-C-T

169902422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333827-A-G

169902597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333648-C-T

169902637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333608-G-C

169902645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333600-G-A

169903527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333319-G-A

169903531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333315-G-T

http://identifiers.org/hco/5/GRCh38#169903537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34333309-A-C

169903537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333309-A-G

169903537-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333309-A-T

169903588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34333265-T-A

169904599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332583-C-T

169904886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332295-G-A

169904954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332232-C-T

169904970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332216-G-T

169905014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332173-T-C

169905153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34332049-T-G

169905349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34331927-A-T

169905452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34331827-G-A

169906789-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34330929-G-C

169906908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34330860-A-G

169907132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34330630-G-A

169907609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34330158-A-G

169907891-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329883-C-G

169907907-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329872-G-C

169907934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329817-A-G

169907937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329816-C-G

169907998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329727-C-G

169907998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329727-C-T

169908521-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329211-T-A

http://identifiers.org/hco/5/GRCh38#169908570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34329159-C-A

169908570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329159-C-T

169908742-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329069-T-G

169908780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34329038-T-C

169909035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328883-G-C

169909035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328883-G-T

169909209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328707-A-G

169909308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328590-G-T

169909441-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328433-T-A

169909441-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328433-T-G

169909518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328361-C-T

169909535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328345-T-C

169909555-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328327-T-G

169909682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34328218-C-T

169910197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34327725-C-T

http://identifiers.org/hco/5/GRCh38#169910324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34327594-C-A

169910674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34327281-C-T

169910709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34327247-A-G

169910858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34327115-C-T

169910927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34327048-C-T

169911221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326788-A-G

169911224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326785-G-A

169911246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326742-A-G

169911372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326623-C-T

169911504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326508-C-T

169911632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326378-C-T

169911684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326326-A-G

169911969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34326063-T-C

169912200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34325843-T-C

169912230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34325823-A-T

169912758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34325093-G-T

169913805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34324101-G-A

169913805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34324101-G-T

169913982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34323972-C-T

169914127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34323840-A-T

http://identifiers.org/hco/5/GRCh38#169915748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34323147-C-A

http://identifiers.org/hco/5/GRCh38#169915879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34323015-C-A

169915933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322968-C-G

169916007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322892-G-A

169916008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322891-T-C

169916091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322812-A-G

169916229-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322676-A-T

169916548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322382-T-C

169916587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322354-T-G

169916681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322248-A-T

169916755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34322190-C-T

169917325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34321153-G-A

169917833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34320659-G-A

169917836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34320656-A-G

169918188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34320280-C-G

169918941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319946-T-C

169918962-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319926-T-A

169918963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319925-G-A

169919334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319581-G-A

169919346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319569-T-G

169919376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319543-A-G

169919467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319432-G-T

http://identifiers.org/hco/5/GRCh38#169919626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34319288-C-A

169919626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34319288-C-T

169919950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318963-A-G

169919958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318955-T-C

169920490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318464-C-G

169920490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318464-C-T

169920830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318139-C-G

169920830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34318139-C-T

169921707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34316713-T-C

http://identifiers.org/hco/5/GRCh38#169921999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34316450-A-C

169922256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34316291-A-G

http://identifiers.org/hco/5/GRCh38#169922544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34316051-C-A

169923372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315572-C-T

169923373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315571-G-A

169923373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315571-G-T

169923452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315476-G-A

169923489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315439-A-G

169923510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315418-C-T

169923681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315212-G-A

169923826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34315085-T-C

169924059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34314890-G-T

169924449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34314559-T-C

169924509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34314488-T-C

169924847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34314175-T-A

169924964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34314059-T-C

169925176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313872-C-G

http://identifiers.org/hco/5/GRCh38#169925211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34313858-A-C

169925559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313440-G-A

169925559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313440-G-T

http://identifiers.org/hco/5/GRCh38#169925600-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34313399-A-C

169925879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313114-C-T

169925890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313104-G-A

169925902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313092-G-C

169925958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34313037-T-G

169926093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34312903-G-C

169926276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34312674-C-G

169926423-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34312545-C-G

169926542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34312431-C-T

http://identifiers.org/hco/5/GRCh38#169926595-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34312387-A-C

169926733-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34312290-T-A

169926960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34311755-G-A

169926960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34311755-G-T

169926974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34311741-G-T

169927252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34311537-G-A

169927401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34311377-C-T

169928043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34310636-T-C

169928424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34310208-A-G

169928444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34310191-C-T

http://identifiers.org/hco/5/GRCh38#169928507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34310137-A-C

169929013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34309512-T-A

169929029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34309496-A-G

169929052-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34309473-G-C

169929303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34309248-C-T

169929383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34309164-C-T

http://identifiers.org/hco/5/GRCh38#169930309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34308925-C-A

169930340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308894-A-T

169930375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308857-C-T

169930417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308810-T-C

169930668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308558-T-C

169930822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308418-C-T

169930929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308308-C-T

169931220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34308082-A-G

http://identifiers.org/hco/5/GRCh38#169931449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34307835-C-A

http://identifiers.org/hco/5/GRCh38#169931460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34307824-A-C

169931522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34307774-G-A

169932155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34307296-A-G

169932336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34307111-G-T

169932437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34307042-G-T

169932590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306885-G-A

169932592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306883-C-T

169932697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306769-A-G

169932702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306764-C-G

169932715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306751-G-A

169932859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306589-G-A

169932866-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306582-A-T

169932910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306539-C-T

169932936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306504-A-G

169933131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306318-T-C

169933210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306239-A-G

169933256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306193-C-T

169933393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34306046-A-G

169933500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305951-A-G

169933558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305894-A-T

169933563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305889-C-T

169933792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305636-A-G

169933849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305580-G-A

169934092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305362-T-C

169934211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34305224-C-T

169934749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34304528-G-A

169935275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34304073-T-C

169935439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303903-A-G

169935571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303782-A-G

169935657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303697-T-C

169935778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303577-G-A

169936030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303335-G-A

169936199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303163-T-C

169936253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303109-C-T

169936264-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303081-A-T

169936299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34303038-G-A

169936549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34302803-G-T

169937045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34302322-G-A

169937104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34302287-C-T

169937191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34302204-C-T

169937655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34301825-C-T

169941482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34300443-G-C

169941885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34300070-C-T

169941887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34300068-G-A

169942087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34299869-T-C

169942395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34299561-T-C

169942524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34299432-A-G

169943018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34298999-A-G

169943035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34298982-G-A

169943035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34298982-G-T

http://identifiers.org/hco/5/GRCh38#169943353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34298714-C-A

169944277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297682-A-G

169944395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297563-T-G

169944493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297397-G-A

169944493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297397-G-C

169944622-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297255-A-T

169944701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297179-A-G

169944709-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297171-A-T

169944989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34297009-C-T

169945172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34296828-A-G

169945534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34296478-T-G

169945725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34296021-A-G

169945783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295970-A-G

169945829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295938-G-A

169946145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295675-A-G

169946320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295508-G-A

169946447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295385-G-A

169946632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295223-C-G

169946740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34295111-C-T

169946864-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294992-C-G

169946864-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294992-C-T

169946891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294965-T-C

169946971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294884-T-A

169947098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294759-G-C

169947101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294756-T-C

169947110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294748-C-G

169947523-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294351-C-G

169947532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34294342-C-T

169948013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34293975-C-T

169949509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292633-G-A

169949509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292633-G-T

169949692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292452-A-T

169949866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292282-T-C

169949866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292282-T-G

169949961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292229-C-T

169950021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292151-G-A

http://identifiers.org/hco/5/GRCh38#169950028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34292144-C-A

169950028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292144-C-T

169950032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292140-T-G

169950036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292136-T-A

169950113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292062-G-A

169950146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34292010-T-C

169950381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291761-A-G

169950644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291538-C-G

169950644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291538-C-T

169950952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291243-T-C

169951013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291182-G-A

169951096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291102-C-G

169951248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34291008-G-A

169951312-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34290965-A-G

169952126-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289968-A-T

169952329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289754-A-G

169952573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289557-A-G

169952742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289399-G-T

169952823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289337-A-G

169952921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34289256-G-A

169953594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34288968-G-A

169953598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34288964-G-A

http://identifiers.org/hco/5/GRCh38#169953820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34288751-A-C

169953820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34288751-A-G

169954058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34288008-C-T

169954440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287639-A-G

169954449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287626-C-G

169954449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287626-C-T

169954548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287535-G-T

169954818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287241-C-T

169954897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34287161-C-T

169955111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286966-C-T

169955126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286947-G-T

169955172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286902-G-A

169955172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286902-G-T

169955298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286803-G-T

http://identifiers.org/hco/5/GRCh38#169955336-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34286762-C-A

169955336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286762-C-T

http://identifiers.org/hco/5/GRCh38#169955348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34286739-A-C

169955415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286695-G-A

169955514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286597-G-C

169955693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286422-C-T

http://identifiers.org/hco/5/GRCh38#169955739-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34286377-C-A

169955754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34286362-G-A

http://identifiers.org/hco/5/GRCh38#169955980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34285686-A-C

169956040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285638-A-G

169956040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285638-A-T

169956054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285630-G-A

169956054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285630-G-T

169956199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285489-C-T

169956203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285485-C-T

169956277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285410-C-T

169956352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285336-C-G

169956372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285317-T-C

169956377-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285312-A-T

169956449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285242-A-G

169956464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285236-G-A

169956568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34285134-C-G

169956864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34284849-A-T

169956926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34284789-G-A

169957123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34284604-C-T

169957401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34284361-G-A

169957744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34283966-C-T

169958316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34283447-T-G

169958534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34283244-G-A

169958864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34282921-G-A

169959043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34282734-A-G

169959403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34282562-A-G

169959674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34282304-C-T

169960069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281837-G-T

169960205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281702-G-A

169960244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281664-C-G

169960337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281543-T-C

169960644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281232-C-T

169961093-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34281151-G-C

169961249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280995-A-G

169961379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280865-A-G

169962072-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280524-G-A

169962234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280373-G-A

169962490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280144-G-A

169962532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280101-T-C

169962607-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34280021-G-C

169962755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34279887-G-A

169963242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34279634-C-T

http://identifiers.org/hco/5/GRCh38#169963754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34278719-C-A

169963754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278719-C-G

169963754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278719-C-T

169963787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278675-A-G

169963900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278570-C-T

169964110-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278360-C-G

169964278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34278177-G-A

169964498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277964-G-A

169964547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277913-G-A

169964614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277848-G-A

169964725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277775-G-A

169964725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277775-G-T

169964795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277732-G-A

169964811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277717-T-C

http://identifiers.org/hco/5/GRCh38#169964833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34277695-A-C

169964927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277615-A-G

169965207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277344-A-G

169965313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277237-G-T

169965342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277204-C-T

169965362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277166-G-A

169965362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277166-G-T

169965403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277111-C-T

169965490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34277030-C-T

169965588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276710-A-G

169965651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276638-C-T

169965710-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276579-C-G

169965710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276579-C-T

169965883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276372-C-T

169965897-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276358-C-G

169966197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276072-G-C

169966251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34276017-A-G

169969666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275585-A-G

169969830-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275403-C-G

169969830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275403-C-T

169969993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275229-T-C

169970007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275212-G-A

169970011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275208-G-T

169970040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275179-T-C

169970046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275173-C-T

169970064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34275155-C-T

169970392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274785-G-A

169970415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274762-G-C

169970884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274265-G-A

169970897-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274252-A-T

169970978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274186-A-T

169970996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274168-G-A

169970996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274168-G-T

169971131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34274027-G-A

169971169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34273991-G-A

169971174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34273986-G-A

169971207-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34273961-G-T

169971240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34273929-A-G

169971562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34273654-T-A

169972319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272924-T-G

169973009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272745-A-G

169973125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272610-G-A

169973149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272583-C-G

169973152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272580-G-T

169973156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272576-G-A

169973156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272576-G-T

169973265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272471-A-G

169973292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272447-G-A

169973292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272447-G-C

169973578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34272202-A-G

169973983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34271826-C-T

169973997-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34271818-G-C

169974403-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34271121-C-G

169974448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34271074-A-G

169974888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34270449-T-C

169975134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34270210-A-G

169975195-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34270148-G-C

169975329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34270019-C-T

169975441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269926-A-G

169975445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269922-G-T

169975455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269912-T-A

169975475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269892-A-G

169975533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269836-C-T

169975754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269611-A-G

169975756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269609-A-G

169975805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269561-G-A

169975830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269538-A-G

169975891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269474-G-A

169975933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269402-T-G

169976000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269355-T-A

169976119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269244-C-T

169976341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34269023-C-T

169976412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268953-A-G

169976535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268788-G-T

169976545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268778-A-G

169977100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268218-T-G

169977246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268071-G-A

169977246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34268071-G-T

169977420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267892-A-G

169977428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267884-T-C

169977452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267859-C-T

169977587-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267715-A-T

http://identifiers.org/hco/5/GRCh38#169978033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34267241-C-A

169978105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267165-T-A

169978137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267133-G-A

169978244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34267029-G-T

169978295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266985-T-A

169978350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266930-C-T

169978418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266830-T-G

169978422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266826-T-G

169978502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266750-G-A

http://identifiers.org/hco/5/GRCh38#169978776-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#34266472-C-A

169979236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34266005-G-C

169979254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34265986-G-A

169979741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34265511-G-A

169979741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 37271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34265511-G-T