53496417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74781036-T-G

http://identifiers.org/hco/4/GRCh38#53496461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74781123-C-A

53496461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74781123-C-T

http://identifiers.org/hco/4/GRCh38#53496529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74781191-A-C

53496529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74781191-A-T

53496545-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74781206-G-T

http://identifiers.org/hco/4/GRCh38#53496595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74781218-C-A

53496595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74781218-C-G

53496613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74781236-A-G

53496613-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74781236-A-T

53496678-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74781294-T-A

53496678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74781294-T-C

53496678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74781294-T-G

53496893-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74782209-A-G

53496978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74782294-T-C

53497248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74782560-C-T

http://identifiers.org/hco/4/GRCh38#53497313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74782629-C-A

53497518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74782808-C-T

53497544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74782833-C-T

53497774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783059-G-A

53497774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783059-G-C

53497783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783068-G-A

53497949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783233-G-A

53498224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783497-T-C

http://identifiers.org/hco/4/GRCh38#53498492-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74783803-A-C

http://identifiers.org/hco/4/GRCh38#53498549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74783883-C-A

53498549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783883-C-T

53498553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783902-A-G

http://identifiers.org/hco/4/GRCh38#53498567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74783936-C-A

53498567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783936-C-G

53498567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74783936-C-T

53498617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784093-C-T

53498674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74784176-G-A

http://identifiers.org/hco/4/GRCh38#53498965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74784451-C-A

53499025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784505-T-G

53499243-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784696-C-G

53499251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784704-T-C

53499277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784729-G-A

53499319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784748-T-C

53499502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784795-G-A

53499615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74784916-G-T

53499888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785190-A-G

53499950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785250-T-C

53499952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785252-T-C

http://identifiers.org/hco/4/GRCh38#53499979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74785270-C-A

53500054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785339-G-T

53500066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785351-T-G

53500073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785359-A-G

http://identifiers.org/hco/4/GRCh38#53500229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74785501-C-A

53500229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785501-C-T

53500269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785542-C-T

53505870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74785939-A-T

53506180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74786215-A-G

53506223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74786308-G-A

53506223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74786308-G-T

53506355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74786780-T-C

53506538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74786941-C-T

53507104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74787800-C-T

http://identifiers.org/hco/4/GRCh38#53507235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74787922-A-C

53507278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74787966-C-T

53507357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74788049-G-A

53507357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74788049-G-T

53507361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74788053-G-T

53507363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74788055-A-G

53507502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74788195-T-C

53507597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74788402-T-C

53507698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74788507-C-T

http://identifiers.org/hco/4/GRCh38#53507936-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74788725-C-A

53507936-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74788725-C-G

53507936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74788725-C-T

http://identifiers.org/hco/4/GRCh38#53507970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74788763-C-A

53508128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74788923-G-A

53508206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 74789001-G-A

53508248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789043-A-T

53508249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789044-G-A

53508299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789072-A-G

53508359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789093-A-G

http://identifiers.org/hco/4/GRCh38#53508372-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74789106-C-A

53508372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789106-C-G

http://identifiers.org/hco/4/GRCh38#53508382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74789115-C-A

53508382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74789115-C-T

http://identifiers.org/hco/4/GRCh38#53508449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74789188-C-A

53508449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789188-C-G

53508449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789188-C-T

53508477-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789220-T-A

53508687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789403-T-G

53508757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789474-G-A

53508899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789625-G-C

http://identifiers.org/hco/4/GRCh38#53508921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74789647-C-A

53509082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789790-T-C

http://identifiers.org/hco/4/GRCh38#53509142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74789851-A-C

53509142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74789851-A-G

53510147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793073-A-G

53510165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793091-C-G

53510188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793114-G-A

53510205-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793131-A-T

53510469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793401-G-A

53510479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793411-T-G

53510485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793424-G-A

53510638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793580-A-G

53510895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793817-T-C

53511009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793924-G-A

53511009-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74793924-G-C

53511133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794050-A-G

53511151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794065-T-C

http://identifiers.org/hco/4/GRCh38#53511157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74794071-A-C

53511541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794449-G-C

53511755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794672-C-T

53511841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794754-C-G

53511993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794849-T-C

53511995-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794851-G-C

53511995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74794851-G-T

53512539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796106-C-G

http://identifiers.org/hco/4/GRCh38#53512605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74796172-C-A

53512619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796186-G-A

53512690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796216-A-G

53512759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796289-G-A

53512832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796354-T-G

53512842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796364-G-T

53512909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796451-C-T

http://identifiers.org/hco/4/GRCh38#53512920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74796462-C-A

53512920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796462-C-T

53513048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796595-C-T

53513154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796698-C-T

53513185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796730-G-A

53513323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74796871-C-T

53513583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797153-C-T

53513645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797226-C-T

53513663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797244-A-G

53513673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797300-C-T

53513699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797326-C-T

http://identifiers.org/hco/4/GRCh38#53513726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74797341-C-A

53513747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797357-T-A

53514801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74797722-G-A

http://identifiers.org/hco/4/GRCh38#53515517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74798429-C-A

53515517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74798429-C-G

53515517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74798429-C-T

53515619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74798669-A-G

53515627-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74798677-T-A

53515906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74798931-G-T

53516291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799055-T-C

53516320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799080-T-C

53516352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799108-G-T

53516417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799173-T-C

53516636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799416-G-A

53516708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799489-A-G

http://identifiers.org/hco/4/GRCh38#53516825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74799599-C-A

53516825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74799599-C-T

53517333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800283-A-G

53517381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800333-T-C

53517424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800388-C-T

53517527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800487-C-T

53517788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800658-T-C

53517865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800732-C-T

53517897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800764-G-C

53517897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800764-G-T

53518091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74800946-T-A

53518319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74801136-C-T

53518689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74801452-G-T

53518774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74801517-C-T

53518848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74801591-T-G

53519435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802141-A-G

53519480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802171-C-T

53519488-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802179-A-T

53519642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802306-G-A

53519878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802514-G-T

53520034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802678-T-C

53520056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74802694-T-G

53520340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74802985-C-T

53520453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74803100-G-A

53520532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74803179-C-T

53520574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74803221-C-T

http://identifiers.org/hco/4/GRCh38#53520579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74803226-C-A

53520726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74803394-C-T

53521272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74803893-C-T

53521382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804019-G-A

53521382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804019-G-T

53521486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804126-G-A

53521487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804127-T-C

53521510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804146-G-C

53521524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804160-A-G

53521565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74804220-C-G

53523866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74806111-T-C

53524152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74806392-C-T

http://identifiers.org/hco/4/GRCh38#53524201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74806450-C-A

53524201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74806450-C-T

53524726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74807212-C-T

53524773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74807258-T-C

http://identifiers.org/hco/4/GRCh38#53524788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74807264-C-A

53525027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74807447-G-A

53525531-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74808356-C-G

53525533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74808358-A-G

http://identifiers.org/hco/4/GRCh38#53525737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74808544-A-C

53526116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74809467-T-A

53526116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74809467-T-C

http://identifiers.org/hco/4/GRCh38#53526326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74809658-C-A

53526476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74809809-A-G

53526476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74809809-A-T

53526539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74809868-A-G

53527257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74810874-C-T

53529046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74811797-A-G

53529415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812085-G-A

53529439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812109-C-T

53529485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812160-T-C

53529642-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812283-C-G

53529644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812285-A-G

53529746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812383-G-A

http://identifiers.org/hco/4/GRCh38#53529748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74812385-A-C

53529752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812389-A-G

53529840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812456-T-C

53529884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812496-C-G

53529884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812496-C-T

53530147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812708-G-A

53530307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74812879-G-A

53530378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74813034-G-A

53530660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74813503-T-G

53530722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74813586-G-C

53530735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74813599-T-C

53530789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74813791-G-A

53531913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74814846-G-A

53532553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74815239-G-A

53533220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74815823-G-A

53534010-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74816624-T-G

http://identifiers.org/hco/4/GRCh38#53534145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74816717-C-A

53534145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74816717-C-T

53534152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74816724-G-A

53535038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817296-T-C

http://identifiers.org/hco/4/GRCh38#53535325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74817492-C-A

53535341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817507-G-A

53535444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817594-C-T

53535451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817601-G-C

53535495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817645-G-A

53535495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817645-G-T

53535667-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74817974-G-C

http://identifiers.org/hco/4/GRCh38#53535824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74818144-C-A

53535824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74818144-C-G

http://identifiers.org/hco/4/GRCh38#53536454-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74818695-A-C

53536569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74818809-C-G

53537334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74819894-C-T

53537390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74819922-G-C

53537775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820258-C-T

53538005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820481-G-C

http://identifiers.org/hco/4/GRCh38#53538081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74820545-C-A

53538081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820545-C-G

53538081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820545-C-T

53538313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820724-G-T

53538479-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820858-T-G

53538488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820867-G-A

53538501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74820880-T-C

53538662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74821046-C-T

http://identifiers.org/hco/4/GRCh38#53538701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74821085-C-A

53538926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74821315-A-G

53539091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 74821486-A-T

53539104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821499-T-C

53539123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821517-C-T

53539124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821518-G-A

53539124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821518-G-T

53539158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821549-T-C

53539219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821609-C-G

53539219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74821609-C-T

53539659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74821922-A-T

http://identifiers.org/hco/4/GRCh38#53539749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74822027-C-A

53539774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822051-T-C

53539811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822088-T-A

53539915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822198-C-T

53540771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822522-A-G

53540780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822531-C-T

53541392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74822827-A-G

53541476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74822903-A-G

53541739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74823209-G-C

http://identifiers.org/hco/4/GRCh38#53541832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#74823299-C-A

53541838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74823305-T-C

53542190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74823665-T-C

53542397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74824534-T-C

53542505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74824660-T-C

53542774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74824950-A-G

53543023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825220-T-A

53543282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825350-C-G

53543282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825350-C-T

53543485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825499-C-T

53543504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825518-G-A

53543507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825528-G-A

53543557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825571-C-T

53543591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825609-T-A

53543711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825717-T-C

53543756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825768-T-A

53543841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825859-A-G

53543846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825864-C-T

53543851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825869-A-G

53543891-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74825909-T-G

53545024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74826764-T-C

53545031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74826769-T-C

53545040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74826778-G-C

53545051-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74826792-T-A

53545289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74828482-C-T

53545431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74828619-G-A

53545729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74828867-T-C

http://identifiers.org/hco/4/GRCh38#53545801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74828947-C-A

53545801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74828947-C-G

53545801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74828947-C-T

53546139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74829055-G-T

53546198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74829084-T-A

53546198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74829084-T-C

53546572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74829426-G-A

53547013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74829841-G-A

http://identifiers.org/hco/4/GRCh38#53547358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74830110-A-C

53548226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74830770-C-T

http://identifiers.org/hco/4/GRCh38#53549323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74831411-A-C

53549528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74831606-C-T

http://identifiers.org/hco/4/GRCh38#53549536-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#74831614-C-A

53549555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74831633-G-T

53549566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40345
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74831648-G-A