138062320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550253-T-C

http://identifiers.org/hco/3/GRCh38#138062476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99550157-C-A

138062476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550157-C-T

http://identifiers.org/hco/3/GRCh38#138062497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99550138-A-C

138062537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550106-G-T

http://identifiers.org/hco/3/GRCh38#138062558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99550087-C-A

138062558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550087-C-G

138062558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550087-C-T

http://identifiers.org/hco/3/GRCh38#138062578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99550067-C-A

138062578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550067-C-G

http://identifiers.org/hco/3/GRCh38#138062579-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99550066-C-A

138062579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550066-C-T

138062580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550065-T-C

138062616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550035-G-A

138062616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550035-G-C

138062616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550035-G-T

138062652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99550012-T-C

138062682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99549979-G-A

138062682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99549979-G-T

http://identifiers.org/hco/3/GRCh38#138062736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99549925-C-A

138062809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3 prime UTR variant
orthologous variants: 99549861-G-A

138062839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: stop gained
orthologous variants: 99549831-G-A

138062915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: synonymous variant
orthologous variants: 99549752-G-A

138062943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99549724-G-A

138062943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99549724-G-C

http://identifiers.org/hco/3/GRCh38#138063038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99549628-C-A

http://identifiers.org/hco/3/GRCh38#138063064-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99549619-A-C

138063255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99549438-G-T

138063439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99549104-G-A

http://identifiers.org/hco/3/GRCh38#138063452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99549096-A-C

138063517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99549014-A-G

138063677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548891-G-A

138063774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548804-A-G

138063998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548512-C-T

138064017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548493-T-C

138064260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548258-G-A

138064260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548258-G-T

http://identifiers.org/hco/3/GRCh38#138064261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99548257-C-A

138064261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548257-C-T

138064272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548247-A-G

138064278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548241-G-T

http://identifiers.org/hco/3/GRCh38#138064367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99548176-C-A

138064377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548165-G-C

138064378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548164-A-G

138064401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99548143-G-T

138064440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99548100-G-T

138064516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99548015-G-A

138064516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99548015-G-T

138064532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99547996-T-C

138064551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99547974-T-C

138064551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99547974-T-G

138064569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant
orthologous variants: 99547956-A-G

138064592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 99547933-A-G

138064659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99547874-T-C

http://identifiers.org/hco/3/GRCh38#138064698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99547835-C-A

138064698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99547835-C-T

138064798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547735-G-A

138064816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547717-A-T

138064845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547688-G-T

138064873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547618-G-A

138064873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547618-G-C

138064873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547618-G-T

138064875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547616-A-G

http://identifiers.org/hco/3/GRCh38#138064903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99547574-C-A

http://identifiers.org/hco/3/GRCh38#138064905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99547568-C-A

138064905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547568-C-T

138064915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547558-G-C

138064915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547558-G-T

138064919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547554-G-A

138064919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547554-G-T

138064994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547416-G-A

138065221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547128-C-T

138065264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99547069-A-G

138065513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99546627-G-A

138065968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99546195-A-G

138066025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99546139-T-C

138066085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99546071-C-G

138066087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99546069-G-T

138067421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545819-T-C

138067423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545817-A-G

http://identifiers.org/hco/3/GRCh38#138067459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99545799-C-A

138067469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545789-T-A

138067545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545735-G-A

138067545-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545735-G-C

138067557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545723-T-C

138067591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545689-A-G

http://identifiers.org/hco/3/GRCh38#138067604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99545676-C-A

138067607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: synonymous variant
orthologous variants: 99545673-G-A

138067608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545672-G-A

138067620-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545660-G-A

http://identifiers.org/hco/3/GRCh38#138067659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99545621-C-A

138067659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545621-C-T

138067887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545447-C-G

138067918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545418-A-T

138067923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545413-G-T

138067952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545404-G-C

http://identifiers.org/hco/3/GRCh38#138068117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99545242-C-A

138068117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99545242-C-T

http://identifiers.org/hco/3/GRCh38#138068235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99545124-C-A

138068235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense variant
orthologous variants: 99545124-C-T

138068268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, stop_gained
orthologous variants: 99545091-G-A

138068300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99545059-G-A

138068300-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99545059-G-C

138068300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99545059-G-T

138068392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544973-T-C

http://identifiers.org/hco/3/GRCh38#138068422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544941-C-A

138068422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544941-C-T

http://identifiers.org/hco/3/GRCh38#138068494-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544883-A-C

138068494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544883-A-G

138068494-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544883-A-T

138068553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544846-G-A

138068553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544846-G-T

138068609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544794-C-T

138068610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544793-G-A

138068670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544747-T-C

138068674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544743-T-C

138068674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544743-T-G

138068722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544710-C-T

138068728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544704-T-C

138068728-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544704-T-G

138068774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544658-C-T

138068776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544656-G-A

138068827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544608-G-A

138068855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544580-T-C

138068856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544579-G-T

http://identifiers.org/hco/3/GRCh38#138068861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544574-C-A

138068861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544574-C-G

138068861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99544574-C-T

138068916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544520-G-T

http://identifiers.org/hco/3/GRCh38#138068923-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544513-A-C

138068923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544513-A-G

http://identifiers.org/hco/3/GRCh38#138068971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544443-C-A

138069035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99544379-T-C

138069488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544369-T-C

138069556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544310-G-A

http://identifiers.org/hco/3/GRCh38#138069621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99544250-A-C

138069647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544221-G-A

138069764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99544123-C-T

138070483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99543684-C-G

138070608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543536-G-A

138070669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543478-A-T

http://identifiers.org/hco/3/GRCh38#138071495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99543291-C-A

138071495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543291-C-T

http://identifiers.org/hco/3/GRCh38#138071497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99543289-C-A

http://identifiers.org/hco/3/GRCh38#138071558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99543231-A-C

138071558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543231-A-G

138071608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543192-G-T

138071612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99543188-C-T

http://identifiers.org/hco/3/GRCh38#138071634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99543165-C-A

138071692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99543116-C-G

138071748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99543060-C-T

138071798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99543010-A-G

138071807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99543001-A-G

http://identifiers.org/hco/3/GRCh38#138071957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99542876-C-A

138071957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542876-C-G

138071957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542876-C-T

http://identifiers.org/hco/3/GRCh38#138072110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99542741-C-A

138072110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542741-C-T

138072123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542728-G-A

138072415-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542486-T-C

138072467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542432-T-G

138072494-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542405-A-G

138072545-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542337-C-G

138072545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99542337-C-T

138077532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99541793-C-G

138077532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99541793-C-T

http://identifiers.org/hco/3/GRCh38#138077650-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99541666-C-A

138077705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99541611-G-A

138077705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99541611-G-T

http://identifiers.org/hco/3/GRCh38#138077717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99541478-C-A

138077717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99541478-C-G

138077721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99541474-G-A

138077721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99541474-G-T

http://identifiers.org/hco/3/GRCh38#138077722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99541473-C-A

http://identifiers.org/hco/3/GRCh38#138077999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99541169-C-A

http://identifiers.org/hco/3/GRCh38#138078169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99540124-A-C

138078169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99540124-A-G

138078205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99540088-A-G

138080419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99538044-G-T

138080468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537993-G-A

138080468-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537993-G-T

http://identifiers.org/hco/3/GRCh38#138080470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99537991-A-C

138080480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537761-A-G

138080480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537761-A-T

138080488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537753-G-A

138080513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537728-G-A

138080513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99537728-G-C

138080669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537581-C-T

138080690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537556-G-A

138080690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537556-G-T

http://identifiers.org/hco/3/GRCh38#138080693-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99537553-C-A

138080693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537553-C-T

http://identifiers.org/hco/3/GRCh38#138080711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99537535-C-A

138080711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537535-C-T

138080817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537410-G-A

138081476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537202-A-G

138081534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537149-G-A

138081559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537125-C-G

138081633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99537030-A-G

138081689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99536984-G-C

138081689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99536984-G-T

138081720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99536953-G-A

138081787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99536889-G-A

138081787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99536889-G-T

http://identifiers.org/hco/3/GRCh38#138081873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#99536796-C-A

138081873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99536796-C-T

http://identifiers.org/hco/3/GRCh38#138082047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99536610-A-C

138082047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536610-A-G

138082091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536575-C-G

138082136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536530-G-A

138082259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536411-T-G

138082527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99536173-A-G

138082581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536122-T-C

138082628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99536077-C-T

http://identifiers.org/hco/3/GRCh38#138082965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99534926-A-C

138083056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99534838-T-C

138083611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99533763-G-A

138083611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99533763-G-C

138083644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99533729-G-A

138083644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99533729-G-T

138083859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99533329-C-T

138083869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99533319-G-C

138084095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99533123-A-G

138084172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99533046-T-C

138084243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99532975-T-A

138084269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532949-T-C

138084272-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532946-C-G

138084272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532946-C-T

138084498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532486-G-C

138086406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99532167-C-T

138086829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531783-A-G

138086865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531753-T-C

138086873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531745-A-G

138086935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531690-C-T

138086947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531682-C-T

138086977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99531652-A-G

138087053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531576-G-A

138087115-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99531510-T-A

138087821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529773-C-T

138087850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529744-G-A

138087930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529688-T-C

138088053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529605-T-C

138088080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529587-T-C

138088290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529363-T-A

138088290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99529363-T-C

http://identifiers.org/hco/3/GRCh38#138088292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99529361-C-A

http://identifiers.org/hco/3/GRCh38#138088396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/9/GRCm39#99529249-C-A

138088396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529249-C-G

138088396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529249-C-T

138088409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 99529236-A-G

138088452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529193-C-T

138088455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529190-A-G

138088467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529178-T-C

138088467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99529178-T-G

138088543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99529098-G-T

138088545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99529096-T-C

http://identifiers.org/hco/3/GRCh38#138088546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99529095-C-A

138088546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99529095-C-G

138088546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99529095-C-T

138088587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99529073-G-T

http://identifiers.org/hco/3/GRCh38#138088667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99528991-C-A

138088682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528978-G-C

138088698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528956-C-T

138088729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528923-A-G

138088773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528880-C-T

138088832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528822-A-G

138088854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99528803-T-C

138088904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99528748-C-G

138088904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99528748-C-T

138088986-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99528542-C-G

138089171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99528405-C-G

138089318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99528256-G-A

138089403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 99528182-G-T

138089564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 99528029-T-C

http://identifiers.org/hco/3/GRCh38#138089774-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99527831-A-C

138090405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527548-G-A

138090405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527548-G-T

138090480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527478-A-G

138090502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527455-T-C

138090545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527415-G-A

138090751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527141-G-A

138090872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527039-T-C

138090872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99527039-T-G

138091897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99526529-G-T

138092135-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99526317-T-G

138092151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99526301-A-G

138092444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99524684-A-G

138092564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524563-C-T

138092579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524548-T-C

138092617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524510-G-A

138092617-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524510-G-C

138092624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524503-T-C

http://identifiers.org/hco/3/GRCh38#138092658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99524470-C-A

138092659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524469-A-G

138092659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524469-A-T

138092660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524468-T-C

138092663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524465-A-G

138092668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524460-A-G

138094692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524059-T-C

138094751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99524004-C-T

138094764-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99523991-A-T

http://identifiers.org/hco/3/GRCh38#138094858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99523907-C-A

138096406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99523319-A-G

138096545-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99523106-G-A

138096953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99522821-G-A

138096995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99522759-C-T

138097178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99522510-T-A

138097676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99522010-G-T

138097695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99521996-C-T

http://identifiers.org/hco/3/GRCh38#138097725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99521976-C-A

138097725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99521976-C-T

138097754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99521958-T-C

http://identifiers.org/hco/3/GRCh38#138097765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99521947-C-A

138097765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 99521947-C-T

138097789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99521923-C-T

138101201-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99520701-T-A

http://identifiers.org/hco/3/GRCh38#138103023-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99520603-C-A

138103023-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99520603-C-T

138103054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99520569-G-C

138103054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99520569-G-T

138103253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99520339-A-G

http://identifiers.org/hco/3/GRCh38#138103408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99520030-A-C

http://identifiers.org/hco/3/GRCh38#138103481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99519963-C-A

138103481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99519963-C-T

138103643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99519801-T-C

138103703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99519741-G-A

138103877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99519567-C-T

138103929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 99519515-G-A

http://identifiers.org/hco/3/GRCh38#138104074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99519379-C-A

138104082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519371-G-C

138104082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519371-G-T

138104147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519305-G-T

http://identifiers.org/hco/3/GRCh38#138104152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99519299-C-A

138104152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519299-C-T

138104171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519278-T-C

138104187-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519263-A-G

138104208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519243-G-T

138104306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519153-A-G

138104601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519045-G-A

138104635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519011-G-A

138104638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99519008-T-G

138104737-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99518905-T-G

138104757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99518885-T-C

138107659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99517318-G-T

138107812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99517160-T-C

138108228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 99516910-G-A

138108294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516845-G-A

138108294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516845-G-T

138108295-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516844-G-C

138108295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516844-G-T

138108386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516768-G-A

138108692-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516455-G-C

138108925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99516243-T-C

138109274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515538-T-C

138109388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515418-T-A

138109412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515391-T-C

138109415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515388-C-T

138109481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515322-G-A

138109484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515319-C-G

138110531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515292-A-G

138112061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99515130-G-A

http://identifiers.org/hco/3/GRCh38#138112493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99514695-C-A

138112505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 99514683-T-C

138112515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514673-C-T

http://identifiers.org/hco/3/GRCh38#138112558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99514629-C-A

138112560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514627-T-C

138112577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514610-G-A

138112620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514568-C-T

138113023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514482-A-G

138113089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514419-G-C

138113110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514398-T-G

138113320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514249-A-G

138113334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514208-T-C

138113461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 99514092-A-G

http://identifiers.org/hco/3/GRCh38#138113483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99514070-C-A

138113517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514035-G-T

138113531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514021-G-A

138113531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514021-G-C

138113531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99514021-G-T

138113603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99513949-A-G

138113618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99513934-T-C

138113742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99513778-G-A

138114009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99513154-C-G

138114318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99512849-C-T

138114337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99512831-T-C

138114697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron variant
orthologous variants: 99512375-T-C

http://identifiers.org/hco/3/GRCh38#138115048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#99512052-C-A

138115048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, undefined
orthologous variants: 99512052-C-T

http://identifiers.org/hco/3/GRCh38#138115190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#99511910-C-A

138115192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, undefined
orthologous variants: 99511908-G-A

138115282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: intron_variant, undefined
orthologous variants: 99511830-T-C

138115416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99511697-T-C

138115495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 99511655-G-A

138115495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 99511655-G-T

http://identifiers.org/hco/3/GRCh38#138115538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99511638-C-A

138115540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5 prime UTR variant
orthologous variants: 99511636-A-T

http://identifiers.org/hco/3/GRCh38#138115543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99511633-C-A

http://identifiers.org/hco/3/GRCh38#138115644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#99511583-C-A

http://identifiers.org/hco/3/GRCh38#138115768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#99511449-C-A

138115800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26551
most severe consequence: 5 prime UTR variant
orthologous variants: 99511424-G-A