http://identifiers.org/hco/11/GRCh38#65576082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5776278-C-A

65576082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776278-C-T

65576102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776256-G-T

65576108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776250-C-T

http://identifiers.org/hco/11/GRCh38#65576172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5776198-C-A

65576172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776198-C-T

65576193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776177-A-T

http://identifiers.org/hco/11/GRCh38#65576256-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5776094-A-C

65576256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776094-A-G

65576266-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776084-C-T

http://identifiers.org/hco/11/GRCh38#65576295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5776054-C-A

65576295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776054-C-T

65576296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776053-G-A

65576296-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776053-G-C

65576296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5 prime UTR variant
orthologous variants: 5776053-G-T

65576396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 5775953-A-T

65576453-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775888-T-A

65576453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775888-T-C

http://identifiers.org/hco/11/GRCh38#65576462-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5775879-C-A

65576732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775652-G-A

65576794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775593-T-C

65576968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775453-G-A

65576999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775422-G-A

65577215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775205-G-A

http://identifiers.org/hco/11/GRCh38#65577419-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5775006-A-C

65577419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5775006-A-G

65577660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5774734-C-T

65578111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5774366-T-C

http://identifiers.org/hco/11/GRCh38#65578130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5774340-C-A

65578132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5774338-C-T

65578163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5774308-G-A

65578163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5774308-G-T

http://identifiers.org/hco/11/GRCh38#65578178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5774293-C-A

65578222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5774250-T-C

http://identifiers.org/hco/11/GRCh38#65578251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5774181-C-A

65578281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774151-G-A

65578281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774151-G-T

65578292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774132-G-A

65578292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5774132-G-T

http://identifiers.org/hco/11/GRCh38#65578406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5773984-C-A

65578470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773771-C-T

http://identifiers.org/hco/11/GRCh38#65578583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5773519-C-A

65578583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773519-C-T

65578638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773399-C-T

65578642-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773395-C-T

65579015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5773083-G-A

65579110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5773001-G-A

65579110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5773001-G-C

65579110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5773001-G-T

65579119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5772992-G-A

65579119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5772992-G-C

65579119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5772992-G-T

65579144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5772967-G-A

65579144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 5772967-G-T

65579212-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772877-T-G

65579308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5772800-A-G

65579431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense variant
orthologous variants: 5772677-T-C

65579486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5772624-G-A

http://identifiers.org/hco/11/GRCh38#65579584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5772532-C-A

65579584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5772532-C-G

65579584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5772532-C-T

http://identifiers.org/hco/11/GRCh38#65579917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5772055-C-A

65579917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5772055-C-T

65580264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771688-G-A

65580272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771680-C-T

http://identifiers.org/hco/11/GRCh38#65580297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771651-A-C

65580560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771366-G-T

http://identifiers.org/hco/11/GRCh38#65580563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771363-C-A

65580563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771363-C-T

65580573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771353-T-C

65580574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771352-G-A

65580574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5771352-G-T

65580699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771244-G-A

65580709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771234-T-C

65580791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771164-T-C

http://identifiers.org/hco/11/GRCh38#65580793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771162-C-A

65580793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771162-C-G

65580793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771162-C-T

http://identifiers.org/hco/11/GRCh38#65580810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771145-C-A

65580810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771145-C-G

65580810-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771145-C-T

http://identifiers.org/hco/11/GRCh38#65580840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771125-C-A

65580840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771125-C-T

http://identifiers.org/hco/11/GRCh38#65580852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771113-C-A

65580863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771102-T-A

65580867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771098-T-C

65580867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771098-T-G

http://identifiers.org/hco/11/GRCh38#65580898-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5771063-C-A

65580898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5771063-C-G

65580951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5771010-G-A

65580951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5771010-G-T

65581234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense variant
orthologous variants: 5770729-G-A

65581234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense variant
orthologous variants: 5770729-G-T

65581264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant
orthologous variants: 5770699-G-A

65581344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 5770619-A-G

65581390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5770574-G-A

65581390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5770574-G-T

http://identifiers.org/hco/11/GRCh38#65581391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5770573-C-A

65581391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5770573-C-T

65581494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5770481-G-T

http://identifiers.org/hco/11/GRCh38#65581509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5770463-C-A

65581509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron variant
orthologous variants: 5770463-C-T

65581776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5770196-A-G

65581954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 5770036-C-T

65582004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5769986-G-A

65582258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769744-T-G

65582334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5769671-C-T

65582462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769537-C-G

65582473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769526-G-C

65582494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769505-T-G

http://identifiers.org/hco/11/GRCh38#65582512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5769487-A-C

65582512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769487-A-G

65582520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769479-G-C

65582520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769479-G-T

65582528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769471-A-T

65582542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769457-G-A

65582542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769457-G-C

http://identifiers.org/hco/11/GRCh38#65582597-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5769402-A-C

65582601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5769398-C-T

65582626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769357-G-A

65582626-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769357-G-C

65582690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769300-C-T

http://identifiers.org/hco/11/GRCh38#65582717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5769270-C-A

65582717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769270-C-G

65582755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 5769244-C-T

65582766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769233-G-A

65582766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769233-G-C

65582941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5769088-G-A

65583029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768977-T-A

65583055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768935-G-A

65583073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768845-G-A

65583073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768845-G-C

65583190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768728-G-A

65583208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768710-G-A

65583208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768710-G-T

65583209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768709-T-C

65583210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5768708-C-T

65583238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5768680-G-A

65583578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5767884-C-G

http://identifiers.org/hco/11/GRCh38#65583723-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5767730-C-A

65583723-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5767730-C-G

65583723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 5767730-C-T

http://identifiers.org/hco/11/GRCh38#65583780-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5767673-C-A

65583780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767673-C-T

http://identifiers.org/hco/11/GRCh38#65583850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5767605-C-A

65583850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767605-C-T

65583870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767575-G-A

65583870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767575-G-T

65583876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767569-G-A

65583876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767569-G-C

65583876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767569-G-T

65583878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767567-G-A

65583878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767567-G-T

65583884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767557-A-G

65583891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767550-A-G

65584006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767443-T-C

65584010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 5767439-T-A

65584010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 5767439-T-C

65584048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767422-T-C

65584119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767345-G-A

65584119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767345-G-T

http://identifiers.org/hco/11/GRCh38#65584140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5767325-C-A

65584162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767303-G-A

65584162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767303-G-T

65584175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767290-T-C

65584182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767281-A-G

65584192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767271-G-A

65584192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767271-G-T

65584193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767270-G-A

65584193-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767270-G-T

http://identifiers.org/hco/11/GRCh38#65584210-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5767253-A-C

65584210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 5767253-A-G

65584248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5767215-C-T

65584429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5767034-G-A

65584429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5767034-G-C

65584526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5766930-A-G

65584551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5766905-G-T

65584562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5766893-G-T

65584612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5766843-T-A

65584612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5766843-T-C

65584797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766671-G-T

http://identifiers.org/hco/11/GRCh38#65584907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5766559-C-A

65584907-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766559-C-G

65584907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766559-C-T

65584912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766554-G-A

65584912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766554-G-C

65584925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766550-G-A

65584925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766550-G-C

65584925-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766550-G-T

65584942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766535-G-A

65584942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5766535-G-T

http://identifiers.org/hco/11/GRCh38#65585005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5766474-C-A

65585005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766474-C-T

65585103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766376-G-A

65585103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766376-G-C

65585103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766376-G-T

65585178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766301-G-A

65585232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766247-G-A

65585232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 5766247-G-T

http://identifiers.org/hco/11/GRCh38#65585271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5766208-C-A

65585271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766208-C-G

65585271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766208-C-T

65585307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766172-G-A

65585307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766172-G-C

http://identifiers.org/hco/11/GRCh38#65585318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5766161-C-A

65585318-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766161-C-G

65585318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5766161-C-T

65585325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766154-G-A

65585352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766082-G-A

65585352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5766082-G-T

http://identifiers.org/hco/11/GRCh38#65585490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5765941-C-A

65585490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5765941-C-T

65585520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5765911-T-C

65585524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5765907-G-A

65585524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5765907-G-T

65585535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5765896-A-G

http://identifiers.org/hco/11/GRCh38#65585631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5765795-C-A

65585631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765795-C-T

65585696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765738-G-A

65585696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765738-G-T

65585718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765717-G-A

65585718-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765717-G-T

65585860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5765639-G-A

65586641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764213-G-A

65586807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764092-C-T

65586863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5764035-C-T

65586932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5763969-C-G

65588447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5762020-C-T

65588656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 5761857-C-T

65589086-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761532-G-A

65589349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761388-G-A

65589435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761327-C-T

65589489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761275-G-A

65589506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761265-T-C

http://identifiers.org/hco/11/GRCh38#65589660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5761151-C-A

65589660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761151-C-G

65589660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761151-C-T

65589679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761132-T-C

http://identifiers.org/hco/11/GRCh38#65589688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5761123-C-A

65589688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761123-C-G

65589688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5761123-C-T

http://identifiers.org/hco/11/GRCh38#65589779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5761036-C-A

65589779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5761036-C-T

65589801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 5761014-A-G

65589840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760966-A-G

65589877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760930-G-A

65589877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760930-G-T

65589882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760925-T-C

http://identifiers.org/hco/11/GRCh38#65589981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5760829-A-C

65589997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760813-G-A

65590006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760804-G-A

65590006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760804-G-C

65590072-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760743-C-T

65590117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 5760693-T-C

65590226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760583-A-G

65590226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760583-A-T

65590296-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760511-C-G

65590296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760511-C-T

65590305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760502-G-T

65590352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760479-G-A

65590352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760479-G-T

65590374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760457-G-A

65590374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760457-G-T

http://identifiers.org/hco/11/GRCh38#65590413-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5760416-A-C

65590418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760411-C-T

65590607-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760166-C-T

65590615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760155-G-A

65590615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760155-G-T

65590676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760091-G-A

65590676-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760091-G-C

65590676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760091-G-T

65590679-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760088-A-T

65590720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5760045-G-T

http://identifiers.org/hco/11/GRCh38#65591133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5759520-C-A

http://identifiers.org/hco/11/GRCh38#65591151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5759498-C-A

65591151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5759498-C-G

65591151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5759498-C-T

http://identifiers.org/hco/11/GRCh38#65591160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5759489-C-A

65591160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5759489-C-T

http://identifiers.org/hco/11/GRCh38#65591173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5759462-C-A

65591173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5759462-C-G

65591199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5759436-A-G

65591351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5759250-G-A

65591448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5759149-C-T

65591651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5758967-G-C

65591704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5758924-G-T

http://identifiers.org/hco/11/GRCh38#65591810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758847-C-A

http://identifiers.org/hco/11/GRCh38#65591881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758776-A-C

65591890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5758767-G-C

65591890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 5758767-G-T

65592091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 5758581-G-A

65592132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758536-G-C

65592132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758536-G-T

65592194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 5758460-T-C

65592291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5758363-G-A

65592291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 5758363-G-C

65592343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5758315-G-A

65592343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5758315-G-T

http://identifiers.org/hco/11/GRCh38#65592347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758311-C-A

http://identifiers.org/hco/11/GRCh38#65592433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758258-C-A

65592433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5758258-C-G

65592433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5758258-C-T

http://identifiers.org/hco/11/GRCh38#65592465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758227-C-A

65592465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 5758227-C-T

65592482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3 prime UTR variant
orthologous variants: 5758204-G-A

65592482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3 prime UTR variant
orthologous variants: 5758204-G-T

http://identifiers.org/hco/11/GRCh38#65592495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758193-A-C

http://identifiers.org/hco/11/GRCh38#65592496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#5758192-C-A

65592496-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30682
most severe consequence: 3 prime UTR variant
orthologous variants: 5758192-C-T