6022627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841236-G-A

6022627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841236-G-T

6022652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841214-A-G

6022661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841205-G-A

6022661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841205-G-T

6022662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841204-T-C

6022679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841189-G-A

6022679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841189-G-T

6022719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841151-T-C

http://identifiers.org/hco/7/GRCh38#6022727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143841143-C-A

6022727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841143-C-T

6022735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841135-G-A

6022735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841135-G-T

6022774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841101-T-A

6022779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841096-G-A

6022779-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841096-G-C

6022779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841096-G-T

http://identifiers.org/hco/7/GRCh38#6022824-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143841060-A-C

6022824-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841060-A-G

6022866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841014-A-G

6022877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841003-G-A

6022877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841003-G-C

6022877-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143841003-G-T

6022892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143840988-G-A

6022892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143840988-G-C

6022892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143840988-G-T

http://identifiers.org/hco/7/GRCh38#6023326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143839983-A-C

6023326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143839983-A-G

6023416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143839893-G-A

6023416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 143839893-G-T

http://identifiers.org/hco/7/GRCh38#6023873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143839481-C-A

6023917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839438-G-T

6023943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839426-G-A

6023955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839416-G-A

6023955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839416-G-T

6023979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839394-T-C

6023994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839380-A-G

6024003-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839371-T-G

http://identifiers.org/hco/7/GRCh38#6024054-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143839324-A-C

6024232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839184-G-A

6024260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 143839159-C-T

http://identifiers.org/hco/7/GRCh38#6024357-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143839063-C-A

6024357-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143839063-C-T

6024374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143839051-G-A

6024374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143839051-G-T

6024474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143838978-T-A

6024509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143838943-G-T

6024649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143838776-C-G

http://identifiers.org/hco/7/GRCh38#6024675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_lost
orthologous variants: http://identifiers.org/mco/5/GRCm39#143838755-A-C

6024767-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143838635-T-C

6026798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143835993-C-T

6026834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143835957-C-G

http://identifiers.org/hco/7/GRCh38#6026978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143835815-A-C

6026978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143835815-A-G

6026978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143835815-A-T

http://identifiers.org/hco/7/GRCh38#6027014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143835781-C-A

6027014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143835781-C-G

6027014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143835781-C-T

6027072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143835733-T-C

http://identifiers.org/hco/7/GRCh38#6027139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143835636-A-C

6027739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143834596-G-A

6028676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143834312-C-G

6028689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143834299-T-C

6028690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 143834298-T-C

6028757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143834265-A-G

6028791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143834221-A-T

6028823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 143834202-T-C

6028885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143834132-T-C

6028913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143834097-C-G

6028913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143834097-C-T

6031278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831905-A-T

6031450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 143831726-T-G

6031567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 143831609-C-T

6031592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, undefined
orthologous variants: 143831587-G-A

6031599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 143831580-C-G

6031648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831542-G-C

http://identifiers.org/hco/7/GRCh38#6031702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143831494-C-A

6031702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831494-C-T

http://identifiers.org/hco/7/GRCh38#6031722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143831470-C-A

http://identifiers.org/hco/7/GRCh38#6031736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143831457-C-A

6031736-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831457-C-G

6031736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831457-C-T

6031787-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831409-T-G

6031852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831345-T-G

6031858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831339-T-C

6032357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831037-G-A

6032359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143831035-G-A

http://identifiers.org/hco/7/GRCh38#6032799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143830492-C-A

6032799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143830492-C-T

6032890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, stop_gained
orthologous variants: 143830398-C-T

6034332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143829898-T-C

http://identifiers.org/hco/7/GRCh38#6034568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143829644-C-A

6034568-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143829644-C-G

6034618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143829595-A-G

6034772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143829436-G-A

http://identifiers.org/hco/7/GRCh38#6035421-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143828681-C-A

6035421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143828681-C-T

6035715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, missense_variant
orthologous variants: 143828389-G-A

6035893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, missense_variant
orthologous variants: 143828211-G-A

6036164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 143827940-T-C

6036223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, missense_variant
orthologous variants: 143827881-C-T

http://identifiers.org/hco/7/GRCh38#6036410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143827693-C-A

6036410-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143827693-C-G

6036461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 143827642-G-T

http://identifiers.org/hco/7/GRCh38#6036535-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143827573-A-C

6037286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826445-G-T

6037349-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826383-T-G

6037355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826377-C-T

6037531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 143826205-G-A

6037531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 143826205-G-T

6037659-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826098-T-A

6037660-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826097-G-A

6037660-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826097-G-T

http://identifiers.org/hco/7/GRCh38#6037670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143826087-C-A

http://identifiers.org/hco/7/GRCh38#6037673-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143826084-A-C

http://identifiers.org/hco/7/GRCh38#6037675-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143826082-A-C

6037675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826082-A-G

6037675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143826082-A-T

6037784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143825932-A-G

6037840-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143825859-C-G

6038706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143823636-C-T

6038721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143823623-T-C

6040527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143822412-A-G

http://identifiers.org/hco/7/GRCh38#6040741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143822189-C-A

6040741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143822189-C-G

6040741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143822189-C-T

http://identifiers.org/hco/7/GRCh38#6040749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143822181-C-A

6040749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron variant
orthologous variants: 143822181-C-T

6040917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense variant
orthologous variants: 143821771-T-C

6040968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143821720-T-A

http://identifiers.org/hco/7/GRCh38#6041062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143821626-C-A

6041062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143821626-C-T

6041236-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143821457-T-A

http://identifiers.org/hco/7/GRCh38#6042312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143821162-A-C

6042435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143821052-A-T

6042449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143821038-T-A

6042449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143821038-T-G

6043022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143820758-C-G

6043022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143820758-C-T

6043067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143820713-T-C

6044207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143819356-G-A

6044594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 143819036-C-T

6044686-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143818948-T-G

http://identifiers.org/hco/7/GRCh38#6044701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143818933-A-C

6044701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 143818933-A-G

6046174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143816235-A-G

http://identifiers.org/hco/7/GRCh38#6046194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143816216-C-A

6046194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143816216-C-T

6046542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814635-G-A

6047104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814379-T-C

6047113-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814366-T-A

6047130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814349-G-A

6047130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814349-G-C

http://identifiers.org/hco/7/GRCh38#6047156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143814341-C-A

6047156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143814341-C-T

6047233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 143814267-G-T

6047241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 143814259-T-C

6047241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 143814259-T-G

6048714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143812617-T-A

6048714-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143812617-T-C

6048819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143812501-A-G

http://identifiers.org/hco/7/GRCh38#6048936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143812395-A-C

6048983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143812055-T-C

http://identifiers.org/hco/7/GRCh38#6049095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143811930-C-A

6049137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143811906-C-T

6049232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143811806-C-T

6049280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143811758-C-G

6049839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810769-T-C

6049842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810766-T-A

http://identifiers.org/hco/7/GRCh38#6049869-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143810739-A-C

6049869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810739-A-G

6049880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810730-G-A

6049880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810730-G-C

6049880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 143810730-G-T

6052923-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143809133-A-T

http://identifiers.org/hco/7/GRCh38#6052929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143809127-C-A

6052952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143809103-G-A

6052974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143809065-A-T

6052992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143809048-T-C

http://identifiers.org/hco/7/GRCh38#6053028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143809015-A-C

6053156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143808898-C-G

6054659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143808724-T-C

6054689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 143808694-G-A

6054783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143808605-T-C

6054794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143808594-A-G

6056648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143805033-G-A

6056648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143805033-G-C

6056648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143805033-G-T

6056702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804979-C-T

6056769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804918-G-A

6056908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804778-C-T

6056956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804735-G-A

6058026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804226-T-C

6058026-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804226-T-G

6058628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804052-T-C

6058630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143804050-G-A

6058786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803929-A-G

http://identifiers.org/hco/7/GRCh38#6058806-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803907-C-A

6058903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803822-G-A

6058903-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803822-G-C

6058903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803822-G-T

6058906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803819-G-A

6058906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 143803819-G-T

http://identifiers.org/hco/7/GRCh38#6058917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803808-C-A

6058917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803808-C-T

http://identifiers.org/hco/7/GRCh38#6058918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803807-A-C

6058918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803807-A-G

6058918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803807-A-T

6058921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803804-T-C

6058921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803804-T-G

6058924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803801-A-G

6058924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803801-A-T

6058927-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803798-G-C

6058927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 143803798-G-T

6058984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143803743-G-A

6058984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143803743-G-C

6058984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 143803743-G-T

http://identifiers.org/hco/7/GRCh38#6059045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803682-C-A

6059045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 143803682-C-T

http://identifiers.org/hco/7/GRCh38#6059090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803637-C-A

6059090-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143803637-C-G

6059090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143803637-C-T

http://identifiers.org/hco/7/GRCh38#6059112-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803613-C-A

6059112-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143803613-C-G

6059112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 143803613-C-T

6059133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 143803593-G-A

6059133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 143803593-G-T

http://identifiers.org/hco/7/GRCh38#6059157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803581-C-A

6059157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 143803581-C-G

6059157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 143803581-C-T

http://identifiers.org/hco/7/GRCh38#6059163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#143803572-C-A

6059163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 143803572-C-T

6059165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143803570-G-A

6059165-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143803570-G-C

6059165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24921
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 143803570-G-T