124954155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37259663-C-T

124954225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5 prime UTR variant
orthologous variants: 37259594-G-A

124954225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5 prime UTR variant
orthologous variants: 37259594-G-C

124954347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 37259474-T-C

124954361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5 prime UTR variant
orthologous variants: 37259460-G-A

124954361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5 prime UTR variant
orthologous variants: 37259460-G-T

124954386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, undefined
orthologous variants: 37259430-T-C

http://identifiers.org/hco/11/GRCh38#124954413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37259378-C-A

124954413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37259378-C-T

124954952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258992-C-T

124954981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258962-G-T

124954991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258948-A-G

124954995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258944-A-G

124955006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258933-A-G

124955010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258929-T-C

124955286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258694-C-T

124955415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 37258575-C-T

124956908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37256011-A-G

124959047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255394-G-A

124959047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255394-G-T

124959088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255353-T-C

124959127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 37255315-T-C

124959281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255161-G-T

124959323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255145-A-G

http://identifiers.org/hco/11/GRCh38#124959367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37255106-C-A

124959367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37255106-C-T

http://identifiers.org/hco/11/GRCh38#124959688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37254039-C-A

124959688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37254039-C-T

http://identifiers.org/hco/11/GRCh38#124959729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37253995-A-C

124959729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37253995-A-G

124959729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37253995-A-T

124959770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37253960-G-A

124959770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37253960-G-T

124959861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37253866-T-C

124959952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: synonymous variant
orthologous variants: 37253775-A-G

124960493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37252932-C-T

http://identifiers.org/hco/11/GRCh38#124960891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37252575-A-C

124961273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37241528-T-C

124961296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37241504-G-A

124961912-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37241229-A-T

124969505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37238946-C-T

http://identifiers.org/hco/11/GRCh38#124971027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37236085-C-A

124971051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37236061-G-C

124971058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37236054-A-G

124971181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37235939-T-C

124972890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37233965-A-G

124973620-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37233086-A-T

124974319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37232896-T-C

124974778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37232105-T-A

124974964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231936-G-T

124974968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231932-G-T

http://identifiers.org/hco/11/GRCh38#124974981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37231919-C-A

http://identifiers.org/hco/11/GRCh38#124975011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37231889-C-A

124975011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231889-C-T

http://identifiers.org/hco/11/GRCh38#124975038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37231863-C-A

124975038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231863-C-T

124975074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231826-T-C

http://identifiers.org/hco/11/GRCh38#124975126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37231774-C-A

124975126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37231774-C-G

124975126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37231774-C-T

124975241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231659-A-G

124975583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37231365-A-G

124976202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37230505-G-A

124976839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37229918-G-A

124976905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37229852-G-T

124977315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37229464-G-C

124977330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37229449-G-A

124977333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37229446-G-T

124986542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37228008-G-A

124986549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37228001-A-G

124986624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227906-T-G

http://identifiers.org/hco/11/GRCh38#124986660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37227867-C-A

124986660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227867-C-T

124986671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227854-G-A

124986671-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227854-G-C

124986671-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227854-G-T

124986675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227850-G-A

124986675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227850-G-T

124987016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227304-T-C

124987025-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37227297-T-G

124987161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37227147-T-C

124987306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: synonymous variant
orthologous variants: 37226960-C-T

124987433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226860-G-A

124987433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226860-G-C

124987457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226836-G-A

124987457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226836-G-T

124987499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226836-G-A

124987568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense variant
orthologous variants: 37226836-G-A

124987967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: stop gained
orthologous variants: 37226566-C-T

124987973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: stop gained
orthologous variants: 37226560-C-T

124988151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37226440-A-G

124988152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37226439-G-A

124988155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37226436-G-A

124988155-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37226436-G-C

124988155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37226436-G-T

124991218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225868-G-C

124991266-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225820-A-T

124991344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225755-T-C

124991344-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225755-T-G

http://identifiers.org/hco/11/GRCh38#124991428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37225670-C-A

124991428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225670-C-T

124991434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225664-A-G

124991524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, missense_variant
orthologous variants: 37225583-C-G

124992175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225354-A-G

124992279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225283-C-T

124992323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225243-C-T

124992376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37225179-G-C

124992614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, missense_variant
orthologous variants: 37224744-G-T

124992628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 37224730-C-T

124992631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, missense_variant
orthologous variants: 37224727-G-T

124992635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, missense_variant
orthologous variants: 37224723-A-G

124993241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, splice_region_variant, synonymous_variant
orthologous variants: 37223957-T-C

124993375-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37223821-A-T

124994352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37222554-G-A

124994780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37222426-A-G

124994886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37222349-G-A

124994894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37222341-C-G

124994894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37222341-C-T

125003826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37215736-T-C

125003826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37215736-T-G

125003857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37215706-T-C

125003884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: synonymous variant
orthologous variants: 37215679-A-G

125004076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37215264-T-C

125004311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37215033-C-T

http://identifiers.org/hco/11/GRCh38#125004566-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37214902-A-C

125004585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37214883-C-T

125004962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37214400-A-G

125004968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37214394-T-C

125004968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37214394-T-G

125005192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: synonymous variant
orthologous variants: 37214194-A-G

http://identifiers.org/hco/11/GRCh38#125005250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37214136-C-A

125005250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37214136-C-T

125013178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37211205-A-G

125013178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 37211205-A-T

125016304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37209204-T-G

http://identifiers.org/hco/11/GRCh38#125016363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37209126-C-A

125016400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37209074-G-A

125016401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37209073-A-G

125016401-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37209073-A-T

125016569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37208706-C-G

125016623-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37208653-A-T

125016979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37208336-G-A

http://identifiers.org/hco/11/GRCh38#125019130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37207048-A-C

125019354-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37206884-T-A

125019556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37206692-A-G

125019644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37206634-A-G

125020125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37206179-G-A

125020185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37206117-G-A

125020529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37205308-G-T

125020667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37205173-C-T

125022068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37203769-C-T

http://identifiers.org/hco/11/GRCh38#125022081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37203756-A-C

125022220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37203649-T-G

http://identifiers.org/hco/11/GRCh38#125022269-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37203600-A-C

125022397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37203471-C-T

125022603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37203261-A-G

125022836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37202988-T-C

125022973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron variant
orthologous variants: 37202812-C-T

125038240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191264-T-C

125038270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191221-A-G

125038270-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191221-A-T

http://identifiers.org/hco/11/GRCh38#125038298-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37191176-A-C

125038298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191176-A-G

http://identifiers.org/hco/11/GRCh38#125038325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37191149-C-A

125038325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191149-C-T

125038386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37191088-A-G

http://identifiers.org/hco/11/GRCh38#125038471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37191004-C-A

125038471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 37191004-C-T

125038531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37190944-A-G

125038615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190857-A-G

125038721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190601-G-A

125038761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190564-T-C

125038761-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190564-T-G

125038771-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190554-T-A

125038809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190510-A-T

125038827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37190492-T-C

125038991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37190339-T-A

125038991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 37190339-T-C

http://identifiers.org/hco/11/GRCh38#125039093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37190238-A-C

125039093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37190238-A-G

http://identifiers.org/hco/11/GRCh38#125039279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37190106-C-A

125039279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37190106-C-T

http://identifiers.org/hco/11/GRCh38#125039297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37190088-C-A

http://identifiers.org/hco/11/GRCh38#125039310-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37190071-A-C

125039319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37190062-T-C

125039326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37190055-C-T

125039327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37190054-A-G

125039429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189804-G-A

125039429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189804-G-T

125039446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189789-T-C

125039511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189734-A-G

125039511-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189734-A-T

125039519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 37189726-T-C

125039583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189671-A-T

125039657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189595-T-G

125039692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189562-A-T

125039824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189469-A-G

125040025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189282-G-T

125040052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189253-G-T

125040114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37189182-C-T

http://identifiers.org/hco/11/GRCh38#125040488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188879-C-A

125040516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37188850-A-G

http://identifiers.org/hco/11/GRCh38#125040532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188833-C-A

125040532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 37188833-C-T

http://identifiers.org/hco/11/GRCh38#125040576-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188789-A-C

125040798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188555-A-G

125040830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188524-A-G

125040830-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188524-A-T

http://identifiers.org/hco/11/GRCh38#125040865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188510-C-A

125040896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188475-A-T

125040898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188473-T-A

125040898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188473-T-C

125040898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 37188473-T-G

125041045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188294-G-A

125041045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188294-G-T

125041060-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188279-A-T

125041129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188247-A-G

125041129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188247-A-T

http://identifiers.org/hco/11/GRCh38#125041145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188231-C-A

125041147-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188229-T-G

125041206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188170-T-A

125041206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188170-T-G

http://identifiers.org/hco/11/GRCh38#125041209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#37188167-C-A

125041209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188167-C-G

125041210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188166-T-C

125041213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188163-G-A

125041213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188163-G-T

125041214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188162-C-G

125041221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25798
most severe consequence: 3 prime UTR variant
orthologous variants: 37188155-T-C