100572895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36504555-G-A

100573265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505060-G-T

100573283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505077-A-G

100573299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505093-G-A

100573299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505093-G-T

100573326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505120-T-G

http://identifiers.org/hco/8/GRCh38#100573651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36505337-A-C

100573651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505337-A-T

http://identifiers.org/hco/8/GRCh38#100573660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36505347-C-A

100573705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505389-T-G

100573737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505417-G-T

100573742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505422-T-C

100573761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505442-G-A

100573761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505442-G-C

100573761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505442-G-T

100573762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505443-G-A

100573762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505443-G-C

100573762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505443-G-T

100573785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505461-A-G

http://identifiers.org/hco/8/GRCh38#100573795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36505471-C-A

100573795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505471-C-T

http://identifiers.org/hco/8/GRCh38#100573804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36505481-C-A

100573804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505481-C-T

100573808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505485-G-A

100573808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505485-G-T

100573836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505513-A-G

100573860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505522-T-C

100573863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3 prime UTR variant
orthologous variants: 36505525-C-T

100573964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 36505623-T-C

100574026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505686-G-A

100574026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505686-G-T

100574031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505691-A-G

100574065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505724-G-T

http://identifiers.org/hco/8/GRCh38#100574070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36505729-C-A

100574070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505729-C-T

100574087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36505746-G-A

100576215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507094-T-C

100576261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507137-C-T

100576584-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507437-A-T

100576846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507669-A-G

100576907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507725-A-G

100576926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507748-A-G

100576937-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507759-T-G

100576949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507770-G-A

100576949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507770-G-T

100576959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507786-G-A

100576959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507786-G-C

100576967-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507794-A-T

100577034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 36507860-G-A

100577035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, missense_variant
orthologous variants: 36507861-T-C

100577089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507915-T-A

100577089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507915-T-C

100577113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507935-G-C

100577113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507935-G-T

100577167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36507987-A-T

http://identifiers.org/hco/8/GRCh38#100577186-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36508005-A-C

100577191-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36508010-T-G

100577213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36508120-C-T

100577216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, undefined
orthologous variants: 36508123-G-A

100577216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, undefined
orthologous variants: 36508123-G-T

100577217-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, undefined
orthologous variants: 36508124-T-A

100577217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, undefined
orthologous variants: 36508124-T-C

100577351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36508309-A-T

http://identifiers.org/hco/8/GRCh38#100581499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36516114-C-A

100581499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516114-C-G

100581515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516136-T-C

100581671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516289-A-T

100581797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516397-T-C

100581903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516487-G-A

100582057-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516614-A-T

100582065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516622-G-A

100582312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36516818-T-G

http://identifiers.org/hco/8/GRCh38#100582323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36516830-A-C

100582370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36516875-C-T

100582681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517147-T-C

100583969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517623-G-T

100584213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517847-T-A

100584213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36517847-T-C

100584306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518430-T-C

100584306-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518430-T-G

http://identifiers.org/hco/8/GRCh38#100584352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36518470-A-C

100584470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36518584-G-T

http://identifiers.org/hco/8/GRCh38#100584677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36518768-C-A

100588753-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523485-G-C

100588753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36523485-G-T

http://identifiers.org/hco/8/GRCh38#100588849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36523572-C-A

100588956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 36523679-C-T

100596114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525033-A-T

http://identifiers.org/hco/8/GRCh38#100596177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36525096-C-A

100596177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525096-C-T

100596238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525151-C-T

100596389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525282-C-T

100596410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525303-G-C

100596531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525407-T-C

100596536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525412-G-A

100596536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525412-G-C

100596536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 36525412-G-T

100596743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, missense_variant
orthologous variants: 36525824-C-T

100596777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 36525858-G-C

http://identifiers.org/hco/8/GRCh38#100596786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36525867-A-C

100596825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 36525906-C-T

100596855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525936-G-A

100596855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525936-G-T

100596856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525937-G-A

100596856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525937-G-T

100596906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525973-A-G

100596906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525973-A-T

http://identifiers.org/hco/8/GRCh38#100596929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36525998-C-A

100596929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36525998-C-T

100599986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527460-G-A

100600104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527570-G-A

100600239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527722-G-A

100600239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527722-G-T

100600247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527733-T-G

100600327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527809-C-G

100600327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527809-C-T

100600469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527942-G-A

100600469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527942-G-T

100600541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36527997-G-A

100600580-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36528034-A-T

100600710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36528493-T-C

100608313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36530801-T-G

100608372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36530852-T-C

http://identifiers.org/hco/8/GRCh38#100608376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36530856-A-C

100608406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36530876-T-C

100608642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36531054-G-A

100608650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36531062-A-G

100608752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36531165-G-A

100608752-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36531165-G-C

100608880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36531976-C-T

http://identifiers.org/hco/8/GRCh38#100609170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36532255-A-C

100609176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532261-A-G

100609422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532511-A-G

100609445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532531-T-G

100609519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532603-G-A

100609519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532603-G-C

100609907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36532996-A-G

100610020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533094-G-T

http://identifiers.org/hco/8/GRCh38#100610056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36533149-C-A

100610056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533149-C-T

http://identifiers.org/hco/8/GRCh38#100610072-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36533169-A-C

100610642-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533725-T-G

100610663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533745-C-G

100610714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533797-G-A

100610760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533841-C-T

100610887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36533956-T-C

100610990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534055-T-C

100611103-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534173-T-C

100611120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534182-T-A

100611202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534263-A-G

100611300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534347-G-A

100611300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534347-G-C

100611930-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534514-C-T

100611944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534526-G-T

100611946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534528-T-A

100611946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534528-T-C

100611974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36534539-C-G

100612012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 36534573-C-T

100612107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36535995-G-A

100612107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36535995-G-T

100612159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36536044-G-A

100612159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36536044-G-T

100612178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36536063-A-T

http://identifiers.org/hco/8/GRCh38#100612234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36536114-C-A

100612234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36536114-C-T

http://identifiers.org/hco/8/GRCh38#100612477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36536329-C-A

100612777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36536644-C-T

http://identifiers.org/hco/8/GRCh38#100612911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36537559-C-A

100612911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36537559-C-T

100612972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36537627-T-C

100613021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 36537680-C-T

100613493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36538401-T-C

100613720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36538646-C-T

http://identifiers.org/hco/8/GRCh38#100617217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36539019-C-A

100617217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539019-C-T

100617285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539109-C-T

100617380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539200-A-G

http://identifiers.org/hco/8/GRCh38#100617473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36539289-C-A

100617473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539289-C-T

100617521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539346-G-A

100617521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539346-G-T

100617550-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539375-C-G

100617578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36539405-C-T

http://identifiers.org/hco/8/GRCh38#100617715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36539538-C-A

100617715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 36539538-C-T

100617725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 36539548-T-C

100618509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36540177-G-A

100618526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36540194-T-G

http://identifiers.org/hco/8/GRCh38#100618636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36540297-C-A

100618636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 36540297-C-T

100618644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 36540305-A-G

100618669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36540330-T-C

100618669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36540330-T-G

100618689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 36540350-G-T

100625591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36542994-G-A

100625591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36542994-G-C

100626288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36543798-T-C

100626288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36543798-T-G

100626314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36543824-G-C

100626626-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544079-A-G

100626658-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544119-T-A

100626662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544123-G-T

http://identifiers.org/hco/8/GRCh38#100626834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36544289-A-C

100626869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544324-T-C

100626968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544403-A-G

100627034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36544472-A-G

100629726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545178-T-C

100629741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545193-A-G

100629765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545218-C-T

100630059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545486-T-C

http://identifiers.org/hco/8/GRCh38#100630090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36545517-A-C

http://identifiers.org/hco/8/GRCh38#100630180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36545587-C-A

100630253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545634-T-C

100630253-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545634-T-G

100630256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545637-A-G

100630296-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545665-T-A

100630296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545665-T-C

100630379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: missense variant
orthologous variants: 36545747-G-C

http://identifiers.org/hco/8/GRCh38#100630491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36545848-C-A

100630491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36545848-C-T

100635759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546833-A-G

100635762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546836-A-G

100635775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546849-G-T

100635831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546857-G-A

100635831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546857-G-T

100635848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546874-G-A

100635848-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546874-G-T

http://identifiers.org/hco/8/GRCh38#100635853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36546879-C-A

100635853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546879-C-T

100635870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36546899-T-C

100636213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547218-T-G

100636230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547235-G-A

100637021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547486-G-A

100637130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547603-C-G

100637309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547679-C-T

100637358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547716-G-T

100637549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36547926-T-C

100642281-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552280-C-G

100642281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552280-C-T

100642307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552313-G-A

100642308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552314-T-C

http://identifiers.org/hco/8/GRCh38#100642373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36552378-A-C

100642549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552557-T-C

100642619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552625-G-A

100642642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552645-A-G

100642648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552651-A-G

100642658-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552662-T-G

100642688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36552689-G-A

100649334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 36555465-G-A

100649340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 36555471-G-A

100649379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555514-G-A

100649381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555516-G-T

100649386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555521-G-A

100649440-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555584-T-A

100649440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555584-T-C

100649440-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555584-T-G

http://identifiers.org/hco/8/GRCh38#100649517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555661-C-A

100649517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36555661-C-T

100649530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36555675-T-A

100649530-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36555675-T-G

http://identifiers.org/hco/8/GRCh38#100649641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555732-C-A

100649641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 36555732-C-T

http://identifiers.org/hco/8/GRCh38#100649667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555752-C-A

100649667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555752-C-T

http://identifiers.org/hco/8/GRCh38#100649700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555784-C-A

100649700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555784-C-T

100649703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555785-T-C

100649703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555785-T-G

http://identifiers.org/hco/8/GRCh38#100649705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555787-C-A

100649705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555787-C-T

http://identifiers.org/hco/8/GRCh38#100649712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555794-C-A

100649712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555794-C-T

http://identifiers.org/hco/8/GRCh38#100649722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555804-C-A

100649722-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555804-C-G

100649722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555804-C-T

http://identifiers.org/hco/8/GRCh38#100649725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#36555807-C-A

100649725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: intron variant
orthologous variants: 36555807-C-T

100663279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5 prime UTR variant
orthologous variants: 36558935-T-C

100663288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5 prime UTR variant
orthologous variants: 36558944-G-A

100663358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5 prime UTR variant
orthologous variants: 36559013-G-A

100663358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5 prime UTR variant
orthologous variants: 36559013-G-T

100663408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5 prime UTR variant
orthologous variants: 36559059-C-G

100663583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28605
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 36559202-A-G