50693240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232623-C-G

50693240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232623-C-T

http://identifiers.org/hco/17/GRCh38#50693252-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94232611-C-A

50693253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232610-A-T

50693264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232600-A-G

50693381-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232486-A-T

50693407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232460-G-T

50693435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94232432-C-T

50693469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94232396-G-A

50693482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94232393-G-T

50693485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94232390-C-T

50693528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94232354-G-T

50693556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232344-A-G

50693562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232338-C-T

50693563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232337-A-G

50693604-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232311-T-C

50693669-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232245-G-T

50693680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232234-G-C

http://identifiers.org/hco/17/GRCh38#50693753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94232162-C-A

50693774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232148-G-T

50693777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232145-T-C

50693811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232106-G-A

50693811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232106-G-T

50693813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232104-T-C

50693833-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 94232084-T-C

50694160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94232069-G-A

50694193-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94232038-T-G

50694210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94232021-T-C

50694259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231976-G-T

50694264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231971-G-A

50694264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231971-G-C

http://identifiers.org/hco/17/GRCh38#50694319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231914-C-A

50694333-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231900-A-T

50694342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231891-G-A

50694342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231891-G-T

http://identifiers.org/hco/17/GRCh38#50694398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231839-C-A

http://identifiers.org/hco/17/GRCh38#50694507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231736-C-A

50694507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231736-C-T

50694541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231706-T-C

50694562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231687-G-T

http://identifiers.org/hco/17/GRCh38#50694607-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231654-C-A

50694632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231630-G-T

50694660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231607-G-T

http://identifiers.org/hco/17/GRCh38#50694707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231560-C-A

50694856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231462-A-G

50694861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231457-T-C

50694970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231347-T-C

http://identifiers.org/hco/17/GRCh38#50695008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231308-C-A

50695008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231308-C-T

50695020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231296-T-C

50695033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231283-G-A

50695038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231278-C-T

http://identifiers.org/hco/17/GRCh38#50695182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231253-C-A

50695182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231253-C-G

50695182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231253-C-T

http://identifiers.org/hco/17/GRCh38#50695183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231252-C-A

50695183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231252-C-T

50695184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231251-A-G

50695245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231237-T-C

50695245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231237-T-G

50695256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231226-A-G

http://identifiers.org/hco/17/GRCh38#50695311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231171-C-A

50695311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231171-C-T

50695312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231170-G-A

50695312-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231170-G-C

50695329-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94231153-A-T

50695351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231132-G-A

50695351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94231132-G-T

50695426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94231058-G-A

50695426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94231058-G-T

50695454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94231030-A-G

http://identifiers.org/hco/17/GRCh38#50695459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231025-C-A

http://identifiers.org/hco/17/GRCh38#50695472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94231012-C-A

50695489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230995-G-A

50695489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230995-G-T

50695554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230956-T-C

http://identifiers.org/hco/17/GRCh38#50695560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230950-C-A

50695590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230920-G-A

http://identifiers.org/hco/17/GRCh38#50695603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230907-C-A

http://identifiers.org/hco/17/GRCh38#50695612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230898-C-A

50695612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230898-C-T

50695630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230881-G-A

50695630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230881-G-C

50695630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230881-G-T

http://identifiers.org/hco/17/GRCh38#50695633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230878-C-A

50695633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230878-C-T

50695663-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230849-T-C

50695666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230846-G-A

50695666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230846-G-T

50695668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230844-T-C

http://identifiers.org/hco/17/GRCh38#50695681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230833-C-A

50695681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230833-C-T

50695699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230816-T-C

http://identifiers.org/hco/17/GRCh38#50695702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230813-A-C

50695729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230788-A-G

50695729-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230788-A-T

50695737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230780-C-T

http://identifiers.org/hco/17/GRCh38#50695762-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230755-C-A

50695768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230749-T-C

50695793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230726-T-C

50695821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230698-G-A

http://identifiers.org/hco/17/GRCh38#50695825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230694-C-A

50695825-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230694-C-G

50695825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230694-C-T

50695835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230684-G-A

http://identifiers.org/hco/17/GRCh38#50695862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230658-A-C

50695862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 94230658-A-G

50695880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230640-T-C

50695883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230637-G-A

50695883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230637-G-C

50695883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230637-G-T

http://identifiers.org/hco/17/GRCh38#50695896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230624-A-C

50695911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 3 prime UTR variant
orthologous variants: 94230609-T-C

50696019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94230501-C-T

50696025-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94230495-T-A

50696025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94230495-T-C

http://identifiers.org/hco/17/GRCh38#50696083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230437-C-A

50696091-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94230429-A-T

http://identifiers.org/hco/17/GRCh38#50696099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94230421-C-A

50696099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94230421-C-T

50696136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94230384-T-A

50696181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94230120-A-G

50696242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94230062-T-A

50696242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94230062-T-C

50696242-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94230062-T-G

50696361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94229966-G-A

50696524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94229847-G-T

50696582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94229794-G-T

http://identifiers.org/hco/17/GRCh38#50696737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94229635-A-C

50696737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94229635-A-T

50696753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94229615-T-A

50696753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94229615-T-C

50696753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 94229615-T-G

http://identifiers.org/hco/17/GRCh38#50696773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94229586-C-A

50696773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94229586-C-T

http://identifiers.org/hco/17/GRCh38#50696823-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94229490-A-C

50696823-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94229490-A-T

50696953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94229332-G-A

50696987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94229298-C-G

50696987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94229298-C-T

50697080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94229205-C-T

50697777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94228602-G-T

50697807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94228572-T-C

http://identifiers.org/hco/17/GRCh38#50699422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94225708-C-A

50699422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225708-C-T

50699449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225681-G-A

50699452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225678-G-A

50699453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225677-C-T

50699470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225660-C-G

50699502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225628-G-A

http://identifiers.org/hco/17/GRCh38#50699511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94225619-A-C

50699526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225607-G-A

50699591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225542-T-C

50699611-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225522-T-A

50699616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225517-A-G

50699625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225508-T-G

50699657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225476-T-C

50699670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225463-A-T

50699700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: synonymous variant
orthologous variants: 94225433-G-A

50699791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225342-A-G

50699848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225285-T-C

50699848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225285-T-G

50699872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225273-T-C

50699875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225270-T-C

50699880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense variant
orthologous variants: 94225265-A-T

50699953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94225204-T-C

50699968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94225185-G-A

50699968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94225185-G-T

50699977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94225176-T-C

50700077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron variant
orthologous variants: 94225063-A-G

50700575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94224866-A-G

50700575-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94224866-A-T

50700610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94224831-C-T

50700653-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94224788-T-C

50700653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94224788-T-G

50700682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94224759-C-T

50700690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94224751-C-T

50701059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94223968-A-G

50701065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 94223962-T-C

50701172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223853-G-A

50701173-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223852-T-G

50701208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223821-G-T

50701506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223537-C-T

50701535-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223508-T-G

50701870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223204-T-C

50701924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94223169-G-C

50702702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94222592-G-C

50703078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94222237-C-T

50703403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94221726-G-A

50703631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94221503-G-A

http://identifiers.org/hco/17/GRCh38#50703779-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94221383-A-C

50703779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94221383-A-G

50704006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94221202-G-A

50704103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94221114-C-G

50706491-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94220112-C-G

50706618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94220096-T-C

50706749-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94219939-A-T

50706965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94219782-G-C

50707130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94219603-C-T

50707361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94219360-T-C

50707524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94219208-C-T

50707556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 94219176-C-T

http://identifiers.org/hco/17/GRCh38#50707621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: non_coding_transcript_exon_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94219111-C-A

50707621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94219111-C-G

50707621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94219111-C-T

50707629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 94219103-T-C

50707649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 94219083-G-A

50707649-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94219083-G-C

50707649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 94219083-G-T

50707656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94219076-T-C

50707656-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94219076-T-G

http://identifiers.org/hco/17/GRCh38#50707698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#94219048-C-A

50707698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5 prime UTR variant
orthologous variants: 94219048-C-T

50707715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5 prime UTR variant
orthologous variants: 94219031-A-G

50707715-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5 prime UTR variant
orthologous variants: 94219031-A-T

http://identifiers.org/hco/17/GRCh38#50707732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94219014-C-A

50707732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94219014-C-T

http://identifiers.org/hco/17/GRCh38#50707743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94219003-C-A

50707743-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94219003-C-G

50707743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94219003-C-T

50707763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218983-G-A

50707763-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218983-G-C

50707763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218983-G-T

http://identifiers.org/hco/17/GRCh38#50707775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94218971-C-A

50707775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218971-C-T

http://identifiers.org/hco/17/GRCh38#50707816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94218929-C-A

50707816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218929-C-G

50707816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218929-C-T

50707817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218928-G-A

50707817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218928-G-T

http://identifiers.org/hco/17/GRCh38#50707824-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94218921-C-A

50707824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218921-C-T

50707831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218914-G-A

50707831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218914-G-T

50707844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218895-C-T

http://identifiers.org/hco/17/GRCh38#50707847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#94218892-C-A

50707847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218892-C-G

50707847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218892-C-T

50707850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218888-G-A

50707876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218862-G-A

50707876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28233
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 94218862-G-T