36355854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78507753-G-A

36355854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78507753-G-C

36355900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78507803-G-A

36355900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78507803-G-C

36355900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78507803-G-T

36356114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78508026-C-T

36356260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78508168-G-A

36356260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78508168-G-T

36356263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78508171-G-A

36356263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 78508171-G-T

http://identifiers.org/hco/2/GRCh38#36356660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78508566-C-A

36356660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78508566-C-G

36356660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78508566-C-T

36356873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78508705-G-T

36357064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78508891-C-T

36357086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78508911-G-A

36357095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78508920-G-A

36357329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509165-T-G

36357467-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509300-G-C

36357467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509300-G-T

36357527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509356-T-C

http://identifiers.org/hco/2/GRCh38#36357814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78509603-C-A

36357829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509621-G-A

36357829-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78509621-G-C

36358156-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78509975-A-T

36358164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78509983-G-T

36358244-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510056-G-C

36358269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510081-T-A

36358269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510081-T-C

36358390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510198-G-A

36358529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510334-T-C

36358789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510701-A-T

http://identifiers.org/hco/2/GRCh38#36358820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78510728-A-C

36358820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510728-A-G

36358836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510747-G-C

36358986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78510871-A-G

36359036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78510936-A-G

36359378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511267-T-C

36359381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511270-T-C

36359420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511302-A-G

36359451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511336-A-G

36359453-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511338-A-T

36359457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511342-G-A

36359493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511363-G-C

36359500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511370-G-C

36359585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511431-C-T

36359587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511433-T-C

36359993-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511758-T-G

36360110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511864-T-C

36360113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511867-T-C

36360210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511931-G-A

36360269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511986-G-A

36360269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78511986-G-C

36360302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512017-A-G

36360320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512035-T-C

36360426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512108-C-T

36360544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512167-A-G

36360645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512272-A-G

http://identifiers.org/hco/2/GRCh38#36360661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78512288-A-C

36360677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512304-T-A

36360692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512320-G-A

36360692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512320-G-T

http://identifiers.org/hco/2/GRCh38#36360748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78512376-A-C

36360777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512405-T-C

36360836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512460-A-T

36360901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512547-C-G

http://identifiers.org/hco/2/GRCh38#36360932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78512576-C-A

36360932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512576-C-T

36361095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512741-C-T

36361096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78512742-A-G

36361601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78513950-G-A

36361941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78514279-C-G

36362404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78514862-C-T

36362625-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515071-G-C

36362811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515205-A-T

36362905-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515305-C-G

36362910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515310-A-T

36363408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515463-A-G

36363465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515517-G-A

36363804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515930-C-T

36363822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78515948-G-T

36363880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516097-A-T

36363949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516170-A-G

36364128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516328-T-C

36364158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516359-T-C

36364272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516527-G-A

36364272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516527-G-C

36364321-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516582-A-G

36364530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516783-G-A

http://identifiers.org/hco/2/GRCh38#36364696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78516871-A-C

36364721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516897-G-C

36364789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516959-A-G

36364800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78516969-A-T

36364924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517087-T-C

36364924-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517087-T-G

36365043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517194-C-T

http://identifiers.org/hco/2/GRCh38#36365218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78517332-A-C

36365571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517469-T-C

36365680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517577-T-C

36365688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517585-G-A

36366147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517720-C-T

36366237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78517814-G-A

http://identifiers.org/hco/2/GRCh38#36366267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78517846-A-C

36366579-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519313-G-C

36366850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519585-C-G

36366902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519640-T-C

36367136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519875-A-G

36367178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519919-G-C

36367202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78519942-C-G

36367304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520044-T-C

36367388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520130-T-C

36367401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520147-A-G

36367431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520176-C-T

36367502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520245-C-G

36367632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520370-T-A

36367632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520370-T-C

36367647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78520385-A-G

http://identifiers.org/hco/2/GRCh38#36367665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78520399-A-C

36367665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78520399-A-G

36367759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78520498-G-T

36368198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78520937-C-T

36368242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78520966-A-G

36368346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521026-C-T

36368413-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521101-C-G

36368420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521110-C-T

36368430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521120-A-G

36368777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521391-T-C

36368868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521476-G-A

36369059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78521719-T-C

36369517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522162-T-C

36369760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522312-C-G

36369760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522312-C-T

36369893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522475-C-T

36370031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522614-A-G

36370066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522947-T-G

36370100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78522984-G-A

36370222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523115-G-A

36370222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523115-G-T

36370543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523468-T-C

http://identifiers.org/hco/2/GRCh38#36370749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78523680-A-C

36370802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523721-C-T

36370867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523783-C-G

36370867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523783-C-T

36370897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523812-A-G

36370909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78523825-C-T

36371722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78524626-C-T

36371735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78524639-T-C

36371850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524750-G-A

36371850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524750-G-T

36371977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524875-G-A

36371977-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524875-G-T

36372076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524953-A-G

36372076-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78524953-A-T

http://identifiers.org/hco/2/GRCh38#36372263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78525119-A-C

http://identifiers.org/hco/2/GRCh38#36372318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
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/17/GRCm39#78525176-A-C

36372372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78525219-G-A

36372372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78525219-G-C

http://identifiers.org/hco/2/GRCh38#36372525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78525360-C-A

36372558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78525392-G-A

36372558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78525392-G-C

36372637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78525554-T-C

36372946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78525831-C-T

36373042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78525897-G-A

36373192-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526041-G-C

36373264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526109-A-G

36373541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526362-G-A

36373586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526413-G-A

36373743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526594-A-G

36373761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526612-A-G

36373761-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526612-A-T

36373975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526791-T-C

36374194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78526982-T-C

36374365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527122-A-G

36374568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527312-C-T

36374569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527313-C-G

36374569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527313-C-T

http://identifiers.org/hco/2/GRCh38#36374609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78527362-A-C

http://identifiers.org/hco/2/GRCh38#36374631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78527384-A-C

36374657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527410-A-G

36374747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527481-C-T

36374925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527641-G-A

http://identifiers.org/hco/2/GRCh38#36375070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78527797-C-A

36375230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78527943-T-C

36375404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528093-G-A

36375460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528140-C-T

36375681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528327-C-T

36375858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528465-G-T

http://identifiers.org/hco/2/GRCh38#36376017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78528522-A-C

36376032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528537-G-C

36376509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78528979-G-C

36376681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78529133-G-A

36376707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78529158-T-G

http://identifiers.org/hco/2/GRCh38#36376869-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78529330-C-A

36377093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78529518-C-G

http://identifiers.org/hco/2/GRCh38#36377539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78529904-C-A

36377539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78529904-C-T

36377586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78529949-A-G

36377631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78529984-G-C

36377672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530025-A-G

36377738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530091-G-C

36377738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530091-G-T

36377883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530211-A-T

36378213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530556-A-G

http://identifiers.org/hco/2/GRCh38#36378278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78530614-C-A

36378333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530666-G-A

36378333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530666-G-T

36378425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530735-C-G

36378425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530735-C-T

http://identifiers.org/hco/2/GRCh38#36378434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78530744-C-A

36378434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530744-C-G

36378434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530744-C-T

36378509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530829-A-G

36378509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530829-A-T

36378630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530867-G-A

36378630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530867-G-T

http://identifiers.org/hco/2/GRCh38#36378636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78530876-A-C

http://identifiers.org/hco/2/GRCh38#36378637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78530877-C-A

36378639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530879-G-A

36378639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530879-G-T

http://identifiers.org/hco/2/GRCh38#36378640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78530880-C-A

36378640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530880-C-T

36378641-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530881-T-A

36378641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530881-T-C

36378645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78530885-C-G

36378971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531119-G-T

36379000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531142-A-G

36379000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531142-A-T

36379008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531150-T-G

36379052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531198-C-T

36379252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531404-G-A

http://identifiers.org/hco/2/GRCh38#36379330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78531482-C-A

36379330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78531482-C-G

36379539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531685-G-A

36379545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531691-G-A

36379615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78531798-T-C

36379962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532115-G-A

36380002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532151-A-G

36380153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532297-A-G

36380406-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532480-C-G

36380852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532890-G-A

36380938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78532964-C-T

http://identifiers.org/hco/2/GRCh38#36381039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78533057-A-C

36381206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78533209-G-A

36381272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78533276-G-A

36381272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78533276-G-T

36381424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78533421-C-T

36381472-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78533469-A-G

36381923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78533709-T-C

36381991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78533763-C-T

36382424-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78534171-C-G

36382758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78534463-T-C

36382853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78534570-T-C

36383057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78534797-A-G

36383569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535479-A-G

36383838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535728-G-A

36383838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535728-G-T

http://identifiers.org/hco/2/GRCh38#36383927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78535815-C-A

36383927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535815-C-T

36383940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535828-G-A

36383941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78535829-C-T

36384213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78536050-C-T

36384757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78536140-C-T

36384802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78536190-G-A

36384812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78536200-T-A

36385401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78536871-T-C

36386341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538099-T-C

36386422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538177-C-G

36386422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538177-C-T

36386623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538366-G-T

36386742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538469-G-A

36386896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538560-A-G

36386960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538630-T-C

36387050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538715-C-T

36387282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538917-A-G

36387299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538931-C-T

36387316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78538947-T-G

36388671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539427-G-A

36388671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539427-G-C

36388726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539483-T-A

36388726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539483-T-C

36388912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539923-G-A

36388920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78539930-G-C

36389065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78540057-G-A

36389485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78540471-C-T

36389530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78540516-T-C

36389532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78540518-T-C

36389834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78540787-A-G

36389977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78540918-A-G

36392925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541368-G-A

36393300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541737-T-C

36393326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541769-A-G

36393616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78541971-C-T

36393891-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542312-G-T

36393982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542381-T-C

36394049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542473-T-C

36394070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542494-G-T

36394186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542718-C-G

36394186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78542718-C-T

http://identifiers.org/hco/2/GRCh38#36394277-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78542975-C-A

36394377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543066-T-G

36394414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543107-G-T

36394821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543385-A-G

36394841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543416-C-G

36394841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543416-C-T

36395004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543577-T-C

http://identifiers.org/hco/2/GRCh38#36395257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78543662-C-A

36395322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543699-G-T

36395334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543707-G-T

36395363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543736-T-C

36395402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543775-G-A

36395410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543783-G-A

36395551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543933-T-C

36395589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78543970-C-G

36396393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78544958-A-G

36396491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545053-C-T

36396496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545058-A-G

http://identifiers.org/hco/2/GRCh38#36396497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78545059-C-A

36396497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545059-C-G

36396497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545059-C-T

36396501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545063-T-C

36396511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545073-A-T

36396576-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545135-T-C

36396588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545148-T-A

36396588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545148-T-G

36396821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545391-A-T

36396836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545406-G-A

36396836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545406-G-T

http://identifiers.org/hco/2/GRCh38#36396915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78545467-A-C

http://identifiers.org/hco/2/GRCh38#36396916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78545468-C-A

36396933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545485-T-A

36396933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545485-T-C

36396975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545532-G-C

36397212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78545754-A-G

36397480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546020-C-T

36397490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546030-G-A

36397493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78546033-T-C

36403224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548202-C-G

36403273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548242-C-T

36403383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548313-G-A

36403383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548313-G-C

36403699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548535-T-C

36403905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548751-T-C

36403905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548751-T-G

http://identifiers.org/hco/2/GRCh38#36404026-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78548858-C-A

36404027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548859-A-G

http://identifiers.org/hco/2/GRCh38#36404069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78548886-A-C

36404070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548887-G-A

36404070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548887-G-C

36404080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78548897-G-A

http://identifiers.org/hco/2/GRCh38#36404460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78549193-C-A

36404733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549548-A-G

36404802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549660-T-C

36404802-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549660-T-G

36405125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78549952-A-G

http://identifiers.org/hco/2/GRCh38#36405231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78550063-A-C

36405260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78550079-A-G

36405618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78550358-G-T

36405658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78550399-A-G

36405814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78550544-A-G

36406042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78550971-A-G

36406265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551178-T-C

http://identifiers.org/hco/2/GRCh38#36406623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78551322-C-A

36406623-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551322-C-G

36406623-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551322-C-T

http://identifiers.org/hco/2/GRCh38#36406630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78551329-C-A

36406630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551329-C-G

36406630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551329-C-T

http://identifiers.org/hco/2/GRCh38#36406631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78551330-C-A

36406631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551330-C-T

36406737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551417-T-G

36406853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551522-G-T

36406875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551544-T-C

36407020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551643-A-G

36407215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78551974-G-A

http://identifiers.org/hco/2/GRCh38#36407232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78551991-C-A

36407258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552017-T-C

36407260-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552019-T-G

36407312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552069-C-T

36407437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552173-G-A

36407505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552244-T-C

36407751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552490-G-T

36407765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552504-T-C

36407804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552554-T-A

36407969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552728-A-G

36407995-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552754-G-T

36408034-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552790-A-T

36408054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552807-A-G

36408090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552846-C-G

36408177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552923-C-T

36408237-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78552989-A-T

36408272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553024-G-A

36408272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553024-G-T

36408343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553100-G-A

36408630-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553363-T-G

36408689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553434-A-T

36408744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553495-T-C

36409081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553895-G-A

36409106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78553919-A-G

36409253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78554078-A-G

36409877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78554451-C-G

36409986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78554559-G-C

36409986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78554559-G-T

36410016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78554591-A-G

36410504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555100-G-A

36410704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555305-A-G

36410704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555305-A-T

36410747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555339-A-G

36410986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555813-A-G

36411081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555906-A-T

36411107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555932-C-G

36411150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78555970-G-A

36411633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556269-C-T

36411820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556428-C-T

36412038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556635-T-C

36412124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78556720-G-A

http://identifiers.org/hco/2/GRCh38#36412667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78557286-A-C

36412725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78557372-T-C

36412929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78557663-C-G

http://identifiers.org/hco/2/GRCh38#36413043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78557791-C-A

36413043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78557791-C-T

36413221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78557953-G-A

36413609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558361-C-T

36413640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558392-A-G

36413664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558425-C-G

36414017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558800-T-A

36414024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558807-A-G

36414057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558845-T-C

36414065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78558852-A-G

36414272-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559027-A-T

36414520-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559281-C-G

http://identifiers.org/hco/2/GRCh38#36414523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78559284-A-C

36414553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559314-G-C

36414676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559434-G-A

36414676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78559434-G-T

36414874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560042-A-G

http://identifiers.org/hco/2/GRCh38#36415074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78560229-A-C

36415498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560520-G-A

http://identifiers.org/hco/2/GRCh38#36415863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78560867-C-A

36415863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560867-C-G

36415863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78560867-C-T

36417039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78561872-C-T

36417055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78561888-C-G

36417290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562093-T-G

36417307-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562110-C-G

36417473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562303-G-A

36417490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562320-T-A

36417490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562320-T-G

36417709-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562508-G-A

36417724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562521-C-T

36417725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562522-G-A

36417853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78562638-G-A

36418649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563329-A-G

36418688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563354-A-G

36418711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563377-A-T

36418904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563546-T-G

36418947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563580-A-G

36419036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78563670-T-G

36419299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78563928-G-A

36419498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564442-A-G

36419562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564512-C-T

36419632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78564573-G-A

36419715-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78564649-C-G

http://identifiers.org/hco/2/GRCh38#36419748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78564679-C-A

36419759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78564690-A-T

36419809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564730-G-A

36419821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564742-T-C

36419843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564764-A-G

36419869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78564787-T-C

36420028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565272-G-C

36420054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565297-G-C

36420179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565422-A-G

36420188-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565431-A-T

36420426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565782-G-T

36420477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565837-C-G

36420517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565861-G-A

36420546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565901-C-G

36420654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78565991-G-A

36420982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566539-G-A

36420985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566542-G-A

http://identifiers.org/hco/2/GRCh38#36420991-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78566548-A-C

36420991-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566548-A-T

36421106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566664-G-T

36421299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566857-A-G

36421306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566864-A-G

36421307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78566865-A-G

36421509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567109-G-T

36421840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567630-G-A

36422101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78567884-A-G

36422339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568101-A-G

36422468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568224-A-G

36422563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568315-T-G

36422615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568385-A-G

36422642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568412-G-A

36422647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568417-G-A

36422647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568417-G-T

36423017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78568923-C-T

36423142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569044-C-T

36423177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569079-G-A

36423177-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569079-G-T

36423216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569116-A-G

36423278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78569171-C-T

36423462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569351-T-C

36423588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78569867-G-A

36423714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570013-A-G

36423793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570059-T-C

36423805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570071-C-T

36423963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570389-C-T

36423975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570401-T-C

36423982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570408-A-G

36424104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570514-T-C

36424226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570648-A-G

36424309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570724-A-G

36424456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78570865-T-A

36425492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571135-T-G

http://identifiers.org/hco/2/GRCh38#36425630-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78571265-A-C

http://identifiers.org/hco/2/GRCh38#36425790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78571574-C-A

36425790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571574-C-T

36425856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571640-C-T

http://identifiers.org/hco/2/GRCh38#36425985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78571775-A-C

36426062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571861-G-C

36426062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571861-G-T

36426147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78571971-C-G

http://identifiers.org/hco/2/GRCh38#36426210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78572036-C-A

36426524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572455-G-A

36426524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572455-G-T

36426723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572694-A-G

36426731-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572702-C-G

36426759-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572752-G-C

36426759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572752-G-T

36426762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572789-C-T

http://identifiers.org/hco/2/GRCh38#36427182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78572954-C-A

36427205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78572963-A-G

36427264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573017-G-C

36427466-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573235-T-A

36427603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573352-T-C

36427631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573373-G-T

36427634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573376-T-A

http://identifiers.org/hco/2/GRCh38#36427644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78573386-C-A

36427736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573473-G-A

36427739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573476-C-G

36427739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573476-C-T

36428026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78573716-G-T

36428386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574060-A-G

36428431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574105-A-T

36428490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574170-A-G

36428495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574175-A-G

36428504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574184-C-T

36428604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574246-T-C

36428832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574641-A-G

36428939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574771-G-A

36428939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574771-G-T

36428989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574822-C-T

36429050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574877-A-G

36429086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78574913-A-G

36429210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575036-G-T

36429508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575267-T-C

36429511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575270-A-T

36429666-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575409-T-A

36429667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575410-G-A

36429808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575532-G-A

36429826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575550-T-C

36429865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575581-G-A

36429883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575601-T-C

http://identifiers.org/hco/2/GRCh38#36429970-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78575671-A-C

36430059-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575754-G-C

36430210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78575872-C-T

http://identifiers.org/hco/2/GRCh38#36430504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78576144-C-A

36430705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576367-T-A

36430820-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576435-T-G

36430945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576515-C-T

36431188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78576747-T-A

36431922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578354-C-T

36432198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578615-G-A

36432517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578936-G-A

36432517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578936-G-C

36432537-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578952-T-A

36432540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578955-C-T

36432574-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78578984-A-T

36432602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579005-G-A

36432931-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579294-A-T

36432980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579314-G-A

36433044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579379-G-A

36433086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579420-C-T

36433240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78579581-C-T

36433568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78579865-C-T

36433711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580004-C-T

36433779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580083-A-G

36433877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580173-A-G

36434298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580600-C-T

36434398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580697-C-T

36434422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580711-C-T

36434678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78580975-T-C

http://identifiers.org/hco/2/GRCh38#36434679-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78580976-A-C

36434759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581054-C-T

36434774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581069-A-G

36434946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581349-C-T

36434975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581392-C-T

36435054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581481-G-A

36435083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581520-G-A

36435179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78581703-G-A

36435494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582141-T-C

36435548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582195-T-G

36435630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582241-T-C

36435819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582386-T-C

36436018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582595-A-G

36436027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582604-G-C

36436127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582713-C-T

36436314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582854-G-C

36436385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78582920-A-G

36436531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583075-G-A

36436551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583095-C-G

36436565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583111-G-A

36436917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583421-A-G

36436917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583421-A-T

http://identifiers.org/hco/2/GRCh38#36437050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78583592-C-A

36437050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583592-C-T

http://identifiers.org/hco/2/GRCh38#36437188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78583758-A-C

36437201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583811-G-A

36437201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583811-G-C

36437234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583871-G-A

36437236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583873-G-A

36437242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583879-G-T

http://identifiers.org/hco/2/GRCh38#36437268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78583904-C-A

36437268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583904-C-G

36437268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78583904-C-T

36437448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584147-G-C

http://identifiers.org/hco/2/GRCh38#36437581-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78584286-A-C

36437700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584407-G-A

36438064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584694-G-A

36438375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78584863-G-A

36438539-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585024-C-G

36438539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585024-C-T

36438572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585056-G-C

36438673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585161-G-C

36438715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585194-A-G

36438739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585218-C-T

36438753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585232-C-G

http://identifiers.org/hco/2/GRCh38#36438796-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78585280-A-C

36438869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585341-G-C

36439314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585771-A-G

36439315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585772-C-T

36439389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585826-G-A

http://identifiers.org/hco/2/GRCh38#36439661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78585903-A-C

36439661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585903-A-G

36439720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585922-C-T

36439777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78585977-G-T

36439897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586072-G-A

36439936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586110-A-G

36440324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586616-A-G

36440520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586756-G-T

36440566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586787-C-T

36440569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78586788-A-G

36440866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587056-C-G

http://identifiers.org/hco/2/GRCh38#36441153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78587296-C-A

36441153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587296-C-T

36441216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587357-C-T

36441388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78587532-C-T

36441424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78587568-G-A

36441564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587706-C-T

36441619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587734-G-A

36441619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587734-G-T

36441711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587820-G-A

36441720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587829-G-A

36441720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587829-G-T

36441791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78587899-A-G

http://identifiers.org/hco/2/GRCh38#36442086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78588180-C-A

36442782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78588845-T-C

36443167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589266-G-T

36443314-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589404-T-G

36443366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589454-A-G

36443672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78589723-G-C

36443960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590507-G-A

36444044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590590-G-A

36444252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590724-A-G

36444287-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590759-A-T

36444348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590816-A-G

http://identifiers.org/hco/2/GRCh38#36444415-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78590888-A-C

36444456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590927-G-T

36444501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78590972-A-T

36445284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78591709-G-A

36445784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592201-G-A

36445920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592311-G-A

36446158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592544-G-C

36446470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592819-C-T

36446591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78592949-C-T

36446705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593050-G-T

36446918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593249-G-A

36446943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593276-A-G

36447183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593477-A-G

36447253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593530-G-A

36447643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78593775-C-T

36447937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594056-T-C

36447986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594088-C-T

http://identifiers.org/hco/2/GRCh38#36448015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78594110-A-C

36448029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594127-C-T

36448093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594190-G-T

36448140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594217-G-A

36448288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594374-G-A

36448856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78594970-T-C

36449080-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595189-T-G

http://identifiers.org/hco/2/GRCh38#36449235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78595332-C-A

36449235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595332-C-T

36449325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595422-G-A

http://identifiers.org/hco/2/GRCh38#36449328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78595425-C-A

36449345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595442-G-A

36449474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595565-G-T

36449638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595680-C-G

http://identifiers.org/hco/2/GRCh38#36449646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78595688-A-C

http://identifiers.org/hco/2/GRCh38#36449805-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78595857-A-C

36449962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595992-G-A

36449962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78595992-G-C

36449990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596020-A-T

36450000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596030-A-G

36450031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596062-T-C

36450043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596069-T-C

36450065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596087-A-G

36450096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596122-A-G

36450177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596216-T-A

36450289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596360-G-A

36450379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596445-T-A

36450481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596534-T-C

36450642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596671-C-T

36450880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596920-G-A

36450893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596933-T-G

36450922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78596969-G-C

36451102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597183-C-T

36451208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597263-A-G

36451249-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597304-C-G

http://identifiers.org/hco/2/GRCh38#36451313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78597351-A-C

http://identifiers.org/hco/2/GRCh38#36451322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78597360-C-A

36451322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597360-C-T

36451490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597593-C-T

36451900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78597983-G-A

36451968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598046-T-C

36452077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598155-A-G

36452219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598290-T-C

36452363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598445-G-A

36452443-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598525-G-C

36452551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598633-T-A

36452551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598633-T-C

36452656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78598739-G-A

36453282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599051-T-G

36453457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599568-G-A

http://identifiers.org/hco/2/GRCh38#36453660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78599743-A-C

36453667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599747-C-T

36453709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78599788-T-C

36453996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600087-G-A

36454284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600383-C-T

36454467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600538-C-G

36454487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600546-T-A

36454495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600554-T-G

36454534-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600565-A-G

36454632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600657-C-T

36454713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600740-A-G

36454817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78600816-T-C

36454994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601014-G-T

36455031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601046-G-A

36455117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601106-G-A

36455129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601118-T-A

http://identifiers.org/hco/2/GRCh38#36455220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78601192-C-A

36455532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601503-G-A

http://identifiers.org/hco/2/GRCh38#36455667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78601590-A-C

36455706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601616-G-T

http://identifiers.org/hco/2/GRCh38#36455736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78601637-A-C

36455896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601819-G-T

36455897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601820-T-G

36455900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601823-A-G

36455969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601892-T-C

36456014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78601933-T-C

36456087-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602005-T-G

36456104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602022-G-T

36456148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602068-C-T

36456180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602111-A-G

36456180-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602111-A-T

36456275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602250-G-C

http://identifiers.org/hco/2/GRCh38#36456316-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78602293-A-C

36456477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602601-C-T

http://identifiers.org/hco/2/GRCh38#36456553-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78602656-A-C

36456578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602682-C-G

36456702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602771-G-T

36456704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78602773-T-A

36457018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603013-C-G

36457046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603035-C-T

36457185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603089-C-T

36457295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603131-C-T

36457423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603256-A-G

36457441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603288-A-G

36457462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603309-G-C

36457462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603309-G-T

36457743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603551-T-C

36457797-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603599-A-G

36457972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603757-T-C

36458140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603898-C-G

36458146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78603904-T-C

36458248-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604000-G-C

36458594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604324-A-G

36458659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604399-G-A

36458692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604431-G-A

36458829-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604572-T-G

36458895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604639-C-T

36459023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604741-A-G

36459095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604810-T-C

36459103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604818-G-A

36459103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78604818-G-T

http://identifiers.org/hco/2/GRCh38#36459258-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78605045-A-C

36459393-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605298-T-G

36459399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605306-G-A

36459418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605325-A-G

36459430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605342-G-C

36459831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605696-A-G

http://identifiers.org/hco/2/GRCh38#36459841-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78605701-A-C

36459905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78605760-T-G

36460058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78605848-C-T

36460111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78605884-A-G

36460114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78605887-G-A

36460267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606063-T-C

36460728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606447-C-G

36460819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606515-A-G

36460911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606587-G-A

36461342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606905-T-A

36461383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78606946-A-T

36461494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607040-G-A

36461780-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607166-T-A

36461780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607166-T-C

36462076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607464-T-C

36462383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607611-T-C

36462394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607622-T-C

36462394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607622-T-G

36462410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607630-G-A

36462451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607666-G-A

36462451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607666-G-T

36462728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78607940-G-A

36462840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78608007-A-G

36462878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78608046-A-G

http://identifiers.org/hco/2/GRCh38#36463034-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78608179-A-C

36463067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78608213-C-T

36463073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78608220-C-T

36463281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609161-G-A

36463397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609274-T-C

http://identifiers.org/hco/2/GRCh38#36463436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78609297-A-C

36463439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609300-G-A

36463439-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609300-G-T

36463556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609419-T-G

36463576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609439-G-A

36463576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609439-G-C

36463610-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609473-T-G

36463875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609736-C-T

http://identifiers.org/hco/2/GRCh38#36463966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78609812-A-C

36464064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78609871-G-A

36464268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610045-G-A

36464325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610108-G-A

36464346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610245-T-C

36464407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610302-A-G

36464735-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610616-T-A

36464735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610616-T-C

36464783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610662-T-G

36464873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610746-G-A

36464874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610747-T-A

36465149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610963-C-T

36465173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78610987-T-C

36465202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611016-C-G

36465202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611016-C-T

36465314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611102-T-C

36465346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611134-A-G

36465346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611134-A-T

36465354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611142-C-G

http://identifiers.org/hco/2/GRCh38#36465374-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78611162-A-C

36465507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611282-T-C

36465660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611429-C-G

36465708-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611472-A-T

36465866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611585-A-G

36466339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611754-A-G

36466516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611980-T-C

36466527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78611993-C-T

36466862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612299-T-C

36466863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612300-A-G

36466922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612354-C-T

http://identifiers.org/hco/2/GRCh38#36466946-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78612378-A-C

36466946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612378-A-G

36467057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612447-C-T

36467159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612514-A-G

36467172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612527-T-C

36467174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612529-G-A

36467308-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612670-A-T

36467468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612804-T-C

36467500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612849-T-C

36467511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612860-C-G

36467512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78612861-A-G

36468069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613549-A-T

36468193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613633-C-T

36468275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613717-A-G

36468399-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613800-G-A

36468399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613800-G-T

36468407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78613808-G-A

36468856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614144-C-T

36468887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78614174-T-A

36468943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78614225-T-C

36468943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78614225-T-G

36468945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78614227-T-C

36469106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78614318-T-C

36469145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614359-T-G

36469181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614395-G-A

http://identifiers.org/hco/2/GRCh38#36469253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78614465-A-C

36469253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614465-A-G

36469267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614479-T-C

36469411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614597-A-T

36469612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614689-G-T

36469725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614777-G-A

36469725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614777-G-T

36469773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614822-A-G

36469777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614826-A-G

36469819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614891-C-T

36469871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614934-C-G

36469871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78614934-C-T

36471966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615323-C-T

36472121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615463-A-G

36472130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615472-A-G

36472209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615533-A-G

36472210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615534-C-T

36472397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615704-G-C

36472664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78615993-A-T

36472675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78616004-G-C

36472724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78616049-A-G

http://identifiers.org/hco/2/GRCh38#36472775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78616094-C-A

36476021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78619051-C-T

http://identifiers.org/hco/2/GRCh38#36476030-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78619060-A-C

36476030-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78619060-A-T

36476119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78619131-A-T

36476123-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78619135-A-T

http://identifiers.org/hco/2/GRCh38#36476465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78619805-C-A

36476665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78619979-G-A

36476731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620036-T-G

36476835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620143-G-T

36476838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620146-A-G

36476932-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78620596-T-A

http://identifiers.org/hco/2/GRCh38#36477092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78620752-C-A

36477092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620752-C-T

36477315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620921-G-A

36477315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78620921-G-C

36477443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621050-G-A

36477686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621243-T-C

36477823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621371-G-A

36477897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621460-G-A

36477969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621531-C-G

36477969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621531-C-T

36478251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621796-T-C

36478372-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78621921-G-C

36478415-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78621963-G-C

36478903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622371-C-T

36479109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622597-G-A

36479152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622639-C-G

36479198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622685-A-G

http://identifiers.org/hco/2/GRCh38#36479355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78622835-C-A

36479355-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622835-C-G

36479355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622835-C-T

http://identifiers.org/hco/2/GRCh38#36479367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78622848-C-A

36479367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622848-C-T

http://identifiers.org/hco/2/GRCh38#36479369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78622850-C-A

36479369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622850-C-T

36479392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622873-A-G

36479392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622873-A-T

36479415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622892-A-G

36479419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622896-A-T

http://identifiers.org/hco/2/GRCh38#36479465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78622946-C-A

36479465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78622946-C-T

http://identifiers.org/hco/2/GRCh38#36479469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78622950-C-A

36479522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623003-C-G

36479522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623003-C-T

36479552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623033-T-A

36479558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623039-C-T

36479621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623102-C-T

36479630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623111-C-G

36479630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623111-C-T

36479666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623147-G-A

36479666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623147-G-C

36479666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78623147-G-T

http://identifiers.org/hco/2/GRCh38#36479748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78623230-C-A

36479777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623262-A-G

http://identifiers.org/hco/2/GRCh38#36479796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78623281-C-A

36479796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623281-C-G

36479799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623284-C-G

36479881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623367-G-A

36479978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623465-A-G

36480027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623514-G-A

36480086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623573-A-G

36480157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623638-A-G

36480293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623778-C-T

36480361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623853-T-C

36480430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623892-G-A

http://identifiers.org/hco/2/GRCh38#36480451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78623913-C-A

36480451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78623913-C-T

36480572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78624190-A-T

36480826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78624475-G-A

36480869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78624502-C-T

36480871-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78624504-C-G

36480907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78624538-A-G

36481497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625010-G-A

36481541-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625046-A-T

36481652-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625162-C-G

36481652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625162-C-T

36481706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625216-G-A

36481912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625365-G-A

36481912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625365-G-C

http://identifiers.org/hco/2/GRCh38#36481992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78625444-C-A

36481992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625444-C-T

36482056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625506-C-G

36482177-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625599-C-G

36482177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625599-C-T

36482241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78625665-T-C

36482693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626118-G-T

http://identifiers.org/hco/2/GRCh38#36482787-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78626208-A-C

36483091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626505-T-A

36483091-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626505-T-G

36483131-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626557-C-G

36483164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626590-C-T

36483224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626936-A-G

36483266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78626977-A-G

36483333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627042-T-C

36483394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627086-A-G

36483495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627173-G-A

36483582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627259-T-C

http://identifiers.org/hco/2/GRCh38#36483625-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78627299-C-A

36483667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627341-A-G

36483912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78627530-G-C

36484432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78628040-A-G

36484889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78628408-T-G

http://identifiers.org/hco/2/GRCh38#36484932-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78628452-C-A

36484932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78628452-C-T

http://identifiers.org/hco/2/GRCh38#36485017-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78628532-A-C

36485017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78628532-A-T

36485638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78629171-A-G

36485932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78629467-A-G

36486309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78629820-G-C

36486389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78629880-G-A

36486615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78630080-G-A

36486615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78630080-G-T

36486621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78630084-G-T

36486884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78630353-C-G

36487255-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78630702-C-G

36487258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78630704-A-G

http://identifiers.org/hco/2/GRCh38#36487538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78631054-C-A

36487558-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631074-T-A

36487647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631165-C-T

36487676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631195-A-G

36487777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631298-A-G

36487905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631390-C-T

36487915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631399-A-G

http://identifiers.org/hco/2/GRCh38#36488271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78631712-C-A

http://identifiers.org/hco/2/GRCh38#36488343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78631778-A-C

36488366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631800-C-G

36488624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78631992-T-C

36488660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632029-C-T

36488728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632096-A-T

36488867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632238-T-C

http://identifiers.org/hco/2/GRCh38#36488946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78632304-C-A

36488979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632338-C-T

http://identifiers.org/hco/2/GRCh38#36488994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78632353-C-A

36488994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632353-C-T

36489268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632719-C-T

36489309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632760-A-G

36489435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78632887-T-C

36489642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78633090-A-T

36489647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78633095-T-G

36490478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78633897-G-A

36490479-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78633898-A-T

36490668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634057-T-C

36491069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634340-C-T

36491317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634541-C-T

36491318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634542-G-A

36491394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634595-C-G

36491424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634625-G-C

36491486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634680-C-T

36491516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634711-C-T

36491519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634714-C-G

36491519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634714-C-T

36491566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634760-A-G

36491599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634799-C-G

36491628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78634828-A-G

36491914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78635128-C-T

36492180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78635398-G-C

36492221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78635439-A-G

36492750-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636006-T-G

36492920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636147-C-T

36492956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636183-G-A

36493285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636366-C-G

36493345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636425-T-C

36493348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636428-G-T

36493357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636437-C-T

36493503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636590-C-T

36493505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636592-G-A

36493567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636653-G-T

http://identifiers.org/hco/2/GRCh38#36493589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78636673-C-A

36493716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78636797-G-A

http://identifiers.org/hco/2/GRCh38#36493788-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78636862-A-C

36493858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637099-A-T

36494015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637301-G-A

http://identifiers.org/hco/2/GRCh38#36494073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78637357-C-A

36494211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637537-G-A

36494586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637742-A-G

36494624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637780-C-T

36494779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78637932-C-T

36494959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638149-G-A

36495171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638309-A-G

36495264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638395-G-A

36495445-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638575-A-T

36495459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638589-C-T

36495616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638711-T-C

36495803-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638927-A-T

36495855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78638966-T-C

36496178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78639220-G-C

36496718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78639754-G-A

36496978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78639992-C-T

36497006-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640020-A-T

36497259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640267-T-C

36497272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640282-C-G

36497280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640290-T-C

36497332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640343-A-T

36497385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640396-T-C

36497455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640467-G-T

http://identifiers.org/hco/2/GRCh38#36497615-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78640631-A-C

36497627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78640645-A-T

36498101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641094-C-T

36498258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641234-G-C

36498258-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641234-G-T

36498260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641236-T-C

36498369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641343-A-G

36498677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641588-G-A

36498763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641680-A-T

36498837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78641747-G-A

http://identifiers.org/hco/2/GRCh38#36499131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78642566-C-A

36499131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78642566-C-T

36499138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78642573-G-A

36499161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78642596-A-G

36499355-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78642792-G-C

36499442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78642887-G-A

36499538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78643003-G-A

36499538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78643003-G-T

36499624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78643104-G-A

36499633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78643113-C-T

36501081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78645497-C-G

36501136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78645551-C-G

36501136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78645551-C-T

36501143-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78645558-C-G

http://identifiers.org/hco/2/GRCh38#36501936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78646025-A-C

http://identifiers.org/hco/2/GRCh38#36502108-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78646193-A-C

36502108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78646193-A-G

36502517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78646593-T-C

36502793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78646807-C-T

36502817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78646842-G-A

36502859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78646884-T-C

36502960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647004-G-A

36503498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647372-G-A

36503617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647445-T-C

http://identifiers.org/hco/2/GRCh38#36503699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78647482-A-C

36503699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647482-A-G

36503870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647641-A-G

36503892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78647660-A-T

36505015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78648505-T-G

36505028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78648518-T-C

36506603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78648820-G-A

36506748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78648969-C-G

36506759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78648979-G-A

36507210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78649081-C-G

36507311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78649170-A-G

http://identifiers.org/hco/2/GRCh38#36507434-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78649285-A-C

36507454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78649298-T-A

36507464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78649308-G-A

http://identifiers.org/hco/2/GRCh38#36507476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#78649320-A-C

36507476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78649320-A-G

36507540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78649381-G-T

36507622-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78649437-T-G

36507634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78649449-C-T

36507980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650135-C-T

http://identifiers.org/hco/2/GRCh38#36508295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78650500-C-A

36508364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650566-C-T

36508469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650670-G-T

36508575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650774-A-G

36508592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650791-G-A

http://identifiers.org/hco/2/GRCh38#36508607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78650798-C-A

36508607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650798-C-T

36508801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78650959-A-G

36508840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651003-C-T

36509091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651228-A-G

36509105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651239-G-A

36509520-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651363-T-G

http://identifiers.org/hco/2/GRCh38#36509528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78651371-C-A

36509528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651371-C-T

36509913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651711-G-A

36509920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651718-A-G

http://identifiers.org/hco/2/GRCh38#36509925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78651723-C-A

36509925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651723-C-T

36509931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651729-G-A

36509941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651739-G-C

36509941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651739-G-T

36509965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651761-G-A

36509965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651761-G-T

36510077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78651873-C-T

36510159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651964-G-A

36510166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651971-T-G

http://identifiers.org/hco/2/GRCh38#36510178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78651984-C-A

36510178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651984-C-G

36510192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651998-G-A

36510192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78651998-G-T

http://identifiers.org/hco/2/GRCh38#36510263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78652073-C-A

36510263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652073-C-T

36510268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652079-T-C

36510269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652080-T-C

36510271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652082-G-A

36510271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652082-G-T

36510276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652087-G-A

36510276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652087-G-C

36510276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652087-G-T

http://identifiers.org/hco/2/GRCh38#36510289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78652100-C-A

36510289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652100-C-T

36511412-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78652269-A-G

36512041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653088-G-T

36512211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653228-T-G

36512212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653229-G-A

36512212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653229-G-T

36512259-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653276-T-A

36512412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653422-G-A

36512428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653438-G-A

36512459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653459-G-A

http://identifiers.org/hco/2/GRCh38#36512462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78653462-C-A

36512462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653462-C-T

http://identifiers.org/hco/2/GRCh38#36512466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78653466-C-A

36512466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653466-C-G

36512525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653526-G-A

36512525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653526-G-T

36512542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653543-T-C

36512657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653638-A-G

36512694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653679-A-G

36512694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653679-A-T

36512745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78653723-T-C

36513174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654161-G-A

36513174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654161-G-T

36513196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654183-A-G

http://identifiers.org/hco/2/GRCh38#36513228-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78654215-A-C

36513268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654251-G-C

36513268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654251-G-T

36513359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654321-T-C

36513359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654321-T-G

36513395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654359-A-G

36513395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654359-A-T

36513431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654401-G-T

http://identifiers.org/hco/2/GRCh38#36513443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78654413-C-A

36513455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654424-G-A

36513455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654424-G-T

http://identifiers.org/hco/2/GRCh38#36513458-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78654427-A-C

36513458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78654427-A-G

36513588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78654538-T-C

36513850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654758-G-A

36513850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654758-G-T

http://identifiers.org/hco/2/GRCh38#36513908-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78654815-C-A

36513915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654822-G-C

36513915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654822-G-T

36513934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78654841-A-G

36514233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655167-C-T

36514337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655252-A-G

36514849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655333-A-G

36514849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655333-A-T

36514884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655359-G-A

36514993-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655454-C-G

36515133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655587-C-G

36515167-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655610-G-C

36515310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78655734-C-T

36515881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78656764-A-G

36515923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78656801-A-G

36516035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78656900-T-C

36516209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657039-A-G

http://identifiers.org/hco/2/GRCh38#36516349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78657161-A-C

36516395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657207-C-T

36516467-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657270-A-T

http://identifiers.org/hco/2/GRCh38#36516474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78657275-A-C

36516474-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657275-A-G

36516474-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657275-A-T

36516583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657351-C-T

36516614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657382-T-C

36516646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657414-A-G

36516661-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657434-C-G

36516661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657434-C-T

36517172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78657941-A-G

36517228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658006-G-A

http://identifiers.org/hco/2/GRCh38#36517270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78658051-C-A

36517382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78658168-T-C

36517578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658364-G-A

36517578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658364-G-T

36517733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658505-C-T

36517789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658553-A-G

36517789-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658553-A-T

36517851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658610-C-T

http://identifiers.org/hco/2/GRCh38#36518015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78658778-C-A

36518015-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658778-C-G

36518106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78658845-T-C

36518280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659039-G-A

36518385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659148-T-C

36518557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659307-G-A

36518652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659345-A-G

36518730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659416-T-G

36518738-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659424-C-G

36518894-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659555-A-T

36518900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659561-G-A

36519037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78659744-G-A

36520468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661001-G-A

36520471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661004-G-C

36520506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661039-A-G

36520790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661168-T-C

36520797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661175-G-A

http://identifiers.org/hco/2/GRCh38#36520858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78661237-A-C

36520858-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661237-A-T

36520914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661293-G-A

http://identifiers.org/hco/2/GRCh38#36520965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78661342-C-A

36521234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661549-G-A

36521379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661676-G-A

36521389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661683-A-G

36521411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661705-T-C

36521477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661768-G-C

36521541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661831-G-A

http://identifiers.org/hco/2/GRCh38#36521663-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78661927-A-C

36521717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661971-C-T

36521732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78661986-G-T

36521911-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662163-T-G

http://identifiers.org/hco/2/GRCh38#36521968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78662247-C-A

36521968-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662247-C-G

36521968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662247-C-T

36522006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662286-G-A

36522014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662294-G-A

http://identifiers.org/hco/2/GRCh38#36522225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78662518-C-A

36522225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 78662518-C-G

36522225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 78662518-C-T

36522328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662621-A-T

36522426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78662725-A-G

36523351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663121-G-T

36523367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663137-C-G

36523367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663137-C-T

http://identifiers.org/hco/2/GRCh38#36523605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78663364-A-C

36523697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663467-C-T

36524024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663581-T-G

36524186-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663726-A-G

36524186-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663726-A-T

36524222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663748-C-T

36524430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78663955-C-T

36524748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664218-A-G

36524871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664338-T-A

36524942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664410-G-A

36525071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664511-C-T

36525112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664546-A-G

36525112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664546-A-T

36525215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664641-T-C

36525487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664905-C-G

36525507-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78664912-G-C

http://identifiers.org/hco/2/GRCh38#36525780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78665169-C-A

36525841-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78665206-G-A

36526203-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78665576-T-G

36526285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78665643-A-G

36526363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78665719-G-A

36526433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78665785-C-T

36526916-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666138-G-C

http://identifiers.org/hco/2/GRCh38#36527148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78666323-A-C

36527148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666323-A-G

36527396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666546-A-G

36527410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666564-A-G

36527432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666592-G-A

36527442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666607-A-T

36527656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78666806-G-C

36528187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667339-C-G

36528187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667339-C-T

36528276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667386-G-A

36528276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667386-G-C

36528467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78667402-G-A

36528594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78667502-C-T

http://identifiers.org/hco/2/GRCh38#36528609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78667518-A-C

36528609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667518-A-G

36528649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667560-G-A

36528668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78667575-C-T

36528707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78667627-G-C

36528772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667695-A-G

36528887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667810-C-T

36528916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667838-A-G

36528917-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78667839-T-G

http://identifiers.org/hco/2/GRCh38#36529118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78668021-C-A

http://identifiers.org/hco/2/GRCh38#36529138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78668044-C-A

36529138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668044-C-G

36529424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78668273-T-C

36529491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78668339-T-C

36529491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78668339-T-G

36529532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668380-C-T

36529534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668382-G-A

36529604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668479-C-T

36529627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668501-G-A

36529627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668501-G-T

36529770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668632-G-C

36530028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78668861-G-C

http://identifiers.org/hco/2/GRCh38#36530353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78669025-C-A

36530426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78669097-G-A

36530454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78669137-G-A

36530456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78669139-G-A

36530957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78669629-G-A

36530957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78669629-G-T

36531047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78669725-G-T

36531440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78670069-C-T

36531689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78670301-G-T

http://identifiers.org/hco/2/GRCh38#36531800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78670392-C-A

36531838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78670431-G-A

36531983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78670608-G-A

36531984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 78670609-C-G

36532071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78670670-G-A

http://identifiers.org/hco/2/GRCh38#36532166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78670766-C-A

36532215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78670817-G-A

http://identifiers.org/hco/2/GRCh38#36533006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78671296-C-A

36533703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78672459-A-G

36533820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78672567-A-G

36533823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78672570-A-G

36534973-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78673781-C-G

36535311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78673881-C-T

36535323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78673893-G-A

36535349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78673920-C-T

36535352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78673923-C-T

36535473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674053-A-G

36535497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674076-A-G

36535501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674080-T-C

36536280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674267-C-G

36536280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674267-C-T

36536325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674301-G-A

36536342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674317-G-C

36536494-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674415-C-G

36536494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674415-C-T

36536793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674647-G-C

36536805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674663-A-G

36536805-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674663-A-T

36536814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674672-G-T

36536879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674733-G-A

36536879-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674733-G-C

http://identifiers.org/hco/2/GRCh38#36537071-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78674924-A-C

36537071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78674924-A-T

36537227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675101-A-G

36537227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675101-A-T

http://identifiers.org/hco/2/GRCh38#36537236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675110-C-A

36537236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675110-C-G

http://identifiers.org/hco/2/GRCh38#36537276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675152-C-A

36537292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675162-T-C

36537292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675162-T-G

36537294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675164-A-G

36537316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675186-A-G

36537320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675190-G-A

36537320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675190-G-T

36537336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675207-C-G

36537407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78675276-C-T

36537413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78675282-G-A

36537437-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78675306-C-G

36537437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78675306-C-T

http://identifiers.org/hco/2/GRCh38#36537554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675423-A-C

http://identifiers.org/hco/2/GRCh38#36537649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675457-C-A

36537649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675457-C-G

36537649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675457-C-T

36537656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675464-G-C

36537656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675464-G-T

36537663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675471-A-G

36537714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675523-A-G

36537848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675650-T-C

36537889-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675691-T-C

http://identifiers.org/hco/2/GRCh38#36537945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675731-C-A

http://identifiers.org/hco/2/GRCh38#36538002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675787-C-A

36538002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675787-C-T

36538013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675798-G-A

36538081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675863-C-G

36538081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675863-C-T

36538174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675934-A-G

http://identifiers.org/hco/2/GRCh38#36538195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78675955-C-A

36538195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78675955-C-G

http://identifiers.org/hco/2/GRCh38#36538230-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78676013-C-A

36538339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78676143-A-G

36538635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78676416-C-T

36540424-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78676810-G-C

36540439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78676825-T-G

36540451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78676837-T-C

36540734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677087-G-A

36540780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677129-G-A

http://identifiers.org/hco/2/GRCh38#36544107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78677155-C-A

36544107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677155-C-G

36544132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677176-A-G

36544155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677190-A-G

36544230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677277-G-A

36544230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677277-G-T

36544283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677325-T-C

36544342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677390-A-G

36544353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677401-G-A

36544353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677401-G-C

36544353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677401-G-T

36544360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677408-T-C

36544532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677578-T-C

36544583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677628-A-G

36544624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677664-T-C

36544645-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677682-T-A

36544645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677682-T-C

36544675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677708-A-G

36544721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677748-G-A

36544739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677766-A-G

36544786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677803-G-A

36544842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677835-G-A

36545019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78677961-G-A

36545070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78678037-C-T

36545133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78678082-A-T

36545302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78678249-C-T

36545504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78678403-A-G

36545567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78678441-G-C

http://identifiers.org/hco/2/GRCh38#36546007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78678859-C-A

36546309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679319-T-C

36546456-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679445-G-C

http://identifiers.org/hco/2/GRCh38#36546589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78679540-A-C

http://identifiers.org/hco/2/GRCh38#36546760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78679781-C-A

36546760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679781-C-G

36546760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679781-C-T

36546768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679789-T-A

36546777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679798-T-C

http://identifiers.org/hco/2/GRCh38#36546793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78679820-C-A

36546793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78679820-C-T

36547039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78680065-T-A

36547039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78680065-T-G

http://identifiers.org/hco/2/GRCh38#36547099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78680125-A-C

36547111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78680137-A-G

http://identifiers.org/hco/2/GRCh38#36547114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78680140-C-A

36547114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 78680140-C-T

http://identifiers.org/hco/2/GRCh38#36547194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78680202-C-A

36547194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680202-C-G

http://identifiers.org/hco/2/GRCh38#36547266-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78680282-A-C

36547266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680282-A-T

36547567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680593-T-C

36547569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680595-G-C

36547598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680616-T-C

36547747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680749-A-G

36547747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78680749-A-T

36548085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78681114-G-A

36548317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78681301-G-T

36548389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78681347-T-A

36548446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78681402-A-G

36548446-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78681402-A-T

36548519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 78681479-A-G

36548570-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 78681530-G-C

http://identifiers.org/hco/2/GRCh38#36548581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78681541-C-A

36548716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78681679-G-A

36548716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78681679-G-T

36548751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78681715-G-C

http://identifiers.org/hco/2/GRCh38#36548752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78681716-C-A

36549134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682105-G-A

36549134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682105-G-T

http://identifiers.org/hco/2/GRCh38#36549185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78682155-C-A

36549185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682155-C-T

http://identifiers.org/hco/2/GRCh38#36549216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78682176-C-A

36549216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682176-C-T

36549222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682182-C-T

http://identifiers.org/hco/2/GRCh38#36549278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78682232-C-A

36549278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682232-C-G

36549278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682232-C-T

http://identifiers.org/hco/2/GRCh38#36549404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78682349-A-C

http://identifiers.org/hco/2/GRCh38#36549490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#78682431-C-A

36549490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682431-C-T

36549513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682449-G-A

36549513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682449-G-T

36549706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78682650-T-C

36550042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683005-T-C

36550046-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683009-T-G

36550070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683033-C-T

36550071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683034-G-A

36550071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683034-G-T

36550121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2359
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 78683085-A-T